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Summary of Results of the Osborn-Ausburn Surname DNA Project

 

Introduction

 

The objective of the project is to try to link families by DNA testing to families that have been able to trace their ancestry to the immigrant families through regular genealogy.  We hope to test as many different families as possible.  Surnames in the project are: Ausburn, Ausborn, Ausburne, Osborn, Osborne, Osburn, Osburne, Ozburn and other variations.

 

The project is hosted by Family Tree DNA and the form for joining and ordering a test is at:

http://www.familytreedna.com/surname_join.asp?code=G48792&special=True

 

Tony Ausburn <tonyausburn@clnk.com> is founder of the group, and he and Thomas Osborne <tlosborne@aol.com> are co-administrators of the group.

 

Below are the results of the tests in terms of genetic distance for each of the 12, 25, 37, and 67 marker tests that have been completed.  Under each table is the interpretation of the genetic distance as copied from the FTDNA web site, followed by a brief summary of the interpretation of the results, and then by the actual alleles.

 

The ancestral lines of most members of the project shown in the Family Group pages, so that if anyone thinks they might be related to any of these lines, they can verify that by getting a DNA test.  Links to the Family Group pages are shown in the navigation bar on the left of web pages, and also in the Genetic distance results tables across the top and Allele tables.  Within the genetic distance tables, clicking on the dash on any diagonal box will link to the appropriate Family Group page for that person. 

 

If a new member’s test doesn’t produce a match to a Family Group already tested, then another Family Group to be added for them.  We certainly welcome anyone who wants to join the project.  These tests have already enabled several of us to leap over our “brick walls” and find our ancestors. 

 

For the history of updates to this site, see the Site Status page.

 

 

Genetic Distance Results

 

The results in the genetic distance tables were taken directly from the FTDNA individual reports of genetic distances to other members of the project.  Note that those in Family Groups 6, 7, 9, and 11 have genetic distances of over 10 to most of the other members of the project.  At first glance, one might wonder how there can be a distance of as much as 12 when only 12 markers were tested; this might lead one to think that every marker must have a different value from the other person in the group, but that is not the case as shown in the Allele table.  The answer is that Allele differences of 2 or more give greater genetic distances than their actual differences.  There are complicated formulas for calculating the genetic distance for different Allele values which FTDNA uses for these calculations.  The methodology and formulas are explained on their web site at [http://nitro.biosci.arizona.edu/ftDNA/Distance.html ] under the heading “Translating the observed difference in allele sizes into an estimate of the actual number of underlying mutation.   FTDNA makes this calculation and reports the resulting genetic distance when it reports genetic distances to each project member.  Below the tables are FTDNA guidelines for translating the genetic distance numbers into the “Relatedness” of the two individuals.

 

What does it mean when two people who think they are related have genetic distance results that indicate they are not related?  These are the possibilities: 1) Both people are related, but an exceptional number of mutations has taken place in one or both lines since the presumed common ancestor.  To my knowledge no one has ever documented a number of mutations that greatly exceeds FTDNA guidelines.  2) There is an error in the dna test results made by the lab that does the analysis for FTDNA.  Many people run into this problem of unexpected results, and the labs have learned to be very careful with many cross checks.  It's possible but very unlikely.  3) There is an error in someone's genealogy.  4) There is a "false-paternity" event in someone's lineage.  A false-paternity event is simply where the true biological father is not who he is supposed to be.  It is believed to happen fairly often, and I think the current belief is as high as 10 to 20% of the time.  Almost by definition, this is a previously unknown event.  When the paper genealogy shows a solid record, this is the explanation most commonly used for this type of situation.  When these situations occur it can be quite disappointing, perhaps upsetting, to the people involved who have usually invested heavily in finding their ancestors.  On the other hand, these results can be extremely valuable in getting research back on the right track or discovering a false paternity.

 

FTDNATiPTM

 

FTDNA has introduced a new program which calculates and displays the probability that two individuals share a common ancestor within the last 100, 200, 300, 400, 500, and 600 years (The same results are now listed in terms of 4, 8, 12, 16, 20, and 24 generations).  The program, called FTDNATiPTM, uses new, and as yet unpublished, mutation rates for each marker.  Consequently the computed probabilities vary with the individuals involved even though their genetic distances may be the same as another pair of individuals.  The only results that are always the same are those for a genetic distance of 0 because those pairs of individuals have exactly the same Alleles on all markers.  FTDNATiPTM, uses a generation length of 25 years and as a result the probability of a common ancestor within a certain number of generations can also be deduced.  In the genetic distance tables, when the cursor is passed over the genetic distance values that are hyperlinked, the Screen Tip under the cursor will show the percentage values in order for 100 to 600 years, or 4 to 24 generations.  To read more about FTDNATiPTM click on the hyperlinked genetic distance numbers.  FTDNATiPTM results are now available to each project member on their own personal FTDNA web page.

 

 

 

 

12 Marker Results


 

Note: So far, James F Osburn and Dale Evert Osborn are the only people in the project with an E1b Haplotype so there is no genetic distance table yet shown for E1b Haplotypes.   they are not related to anyone else in the project or themselves.

 

Table for R1b1 Haplotypes

Table for R1a Haplotypes

Table for I Haplotypes


Click thumbnails for the full 12-marker tables


Distance

Relatedness

Explanation

0

Related

Your perfect 12/12 match means you share a common male ancestor with a person who shares your surname (or variant). These two facts demonstrate your relatedness, however if your name is one of the most common surnames, i.e. Smith, Tailor, Miller, etc, (trades or towns) then we always suggest you utilize our 25 marker test to eliminate the possibility of a random surname and random genetic match.

1

Probably Related

You share the same surname (or a variant) with another male and you mismatch by only one 'point' on only one marker. For most closely related or same surnamed individuals, the mismatch markers are either DYS 439 or DYS 385 A, 385 B and 389-1. Mismatch only in one and you are certain.

2

Probably Not Related

You share the same surname (or a variant) but are off by 2 'points' or 2 locations on just 12 markers. It is only possible that you and another related family members' line each have had a mutation. There are two ways with DNA testing to confirm or deny. One is to test additional family members to search for a line that shows a mutation that is 1 point closer to your sample. The other is to order the Y DNARefine 13-marker panel. Refining greatly enhances sciences ability to determine relatedness -- geared towards the most accurate assessment of the number of generations to a shared ancestor. Only by further testing can you find the person in between each of you...this in 'betweener' becomes essential for you to find, and in their absence we feel you are not related.

3

Not Related

9/12 - is too far off to be considered related. Unlikely but vaguely possible that the rule for Probably Not Related applies.

4

Not Related

8/12 - You are not related and the odds greatly favor that you have not shared a common male ancestor with this person in excess of 2,000 years

5

Not Related

7/12 - You are not related and the odds greatly favor that you have not shared a common male ancestor with this person in excess of 5,000 years.

>5

Not Related

You are totally unrelated to this person.


 

 

 

25 Marker Results

Click for the full 25-marker table

Distance

Relatedness

Explanation

0

Related

Your perfect 25/25 match means you share a common male ancestor with a person who shares your surname (or variant). These two facts demonstrate your relatedness.

1

Related

You share the same surname (or a variant) with another male and you mismatch by only one 'point' on only one marker. For most closely related and same surnamed individuals, the mismatch markers are usually either DYS 439 or DYS 385 A, 385 B,389-1 and 389-2 from our first panel of 12 markers, and on the following from the second panel: DYS #'s 458 459 a 459b 449, 464 a-d, which have shown themselves to move most rapidly. The probability of a close relationship is very high.

2

Probably Related

You share the same surname (or a variant) with another male and you mismatch by two 'point' on from the 25 markers we tested. For most closely related and same surnamed individuals, the mismatch markers are usually either DYS 439 or DYS 385 A, 385 B,389-1 and 389-2 from our first panel of 12 markers, and on the following from the second panel: DYS #'s 458 459 a 459b 449, 464 a-d, which have shown themselves to move most rapidly. The probability of a close relationship is good; however your results show mutations, and therefore more time between you and the other same surnamed person.

3

Probably Not Related

You share the same surname (or a variant) but are off by 3 'points' or 3 locations on the 25 markers tested. If enough time has passed it is possible that you and another distantly related family members' line each have had a mutation, or perhaps 2. The only way to prove that is to test additional family lines and find where the mutation took place. Expressed another way, assume your score puts you at 3 on the clock. Assume the person 3 from you is at the 9 position. Only by further testing can you find the person in between each of you...this in 'betweener' becomes essential for you to find, and in their absence the possibility of a match exists, but further evidence should be pursued.

4

Not Related

21/25 is too far off to be considered related. Unlikely but vaguely possible that the rule for ONLY Possible related applies. It is important to determine what set of result most typifies 'most' members of the group you are 'close' to matching. You may be 21/25 with an individual, but 23/25 with the center (most common) of the group, and your potential relatedness to him is through the center of the group.

5

Not Related

20/25 You are not related and the odds greatly favor that you have not shared a common male ancestor with this person in excess of 2,000 years

6

Not Related

19/25 You are not related and the odds greatly favor that you have not shared a common male ancestor with this person in excess of 5,000 years

>6

Not Related

You are totally unrelated to this person.

 


 

 

 

37 Marker Results

Click for full 37-marker table

Distance

Relatedness

Explanation

0

Very Tightly Related

37/37 Your perfect match means you share a common male ancestor with a person who shares your surname (or variant). Your relatedness is extremely close with the common ancestor predicted, 50% of the time, in 5 generations or less and with a 90% probability within 16 generations. Very few people achieve this close level of a match. All confidence levels are well within the time frame that surnames were adopted in Western Europe.

1

Tightly Related

36/37 You share the same surname (or a variant) with another male and you mismatch by only one 'point' at only one marker--a 36/37 match. It's most likely that you matched 24/25 or 25/25 on a previous Y-DNA test and your mismatch will be found within DYS 576, 570, CDYa or CDYb. Very few people achieve this close level of a match. Your mismatch is within the range of most well established surname lineages in Western Europe.

2

Related

35/37 You share the same surname (or a variant) with another male and you mismatch by only two 'points' --a 35/37 match. It's most likely that you matched 24/25 or 25/25 on previous Y-DNA tests and your mismatch will be found within DYS 439 or DYS 385 A, 385 B,389-1 and 389-2, from our first panel of 12 markers, or from within the second panel at DYS #'s 458, 459 a, 459b, 449, or within 464 a-d. If you matched exactly on previous tests you probably have a mismatch at DYS 576, 570, CDYa or CDYb in our newest panel of markers. Your mismatch is likely within the range of most well established surname lineages in Western Europe.

3

Related

34/37 You share the same surname (or a variant) with another male and you mismatch by three 'points' --a 34/37 match. Because of the volatility within some of the markers this is slightly tighter then being 11/12 or 23/25 and it's most likely that you matched 24/25 or 25/25 on previous Y-DNA tests. Your mismatch will most often be found within DYS 439 or DYS 385 A, 385 B,389-1 and 389-2 from our first panel of 12 markers, or within the second panel: DYS #'s 458, 459 a, 459b, 449, or within 464 a-d. If you matched exactly on previous tests you probably have a mismatch at DYS 576, 570, CDYa or CDYb in our newest panel of markers. Your mismatch is likely within the range of most well established surname lineages in Western Europe.

4

Probably Related

33/37 You share the same surname (or a variant) with another male and you mismatch by four 'points' --a 33/37 match. Because of the volatility within some of the markers this is about the same as being 11/12 and it's most likely that you matched 23/25 or 24/25 on previous Y-DNA tests. If you matched exactly on previous tests you probably have a mismatch at DYS 576, 570, CDYa or CDYb in our newest panel of markers. If several or many generations have passed it is likely that these two lines are related through other family members. That would require that each line had passed a mutation and one person would have experienced at least 2 mutations. The only way to confirm is to test additional family lines and find where the mutations took place. Only by testing additional family members can you find the person in between each of you...this 'in betweener' becomes essential for you to find, and without him the possibility of a match exists, but further evidence must be pursued. If you test additional individuals you will most likely find that their DNA falls in-between the persons who are 4 apart demonstrating relatedness within this family cluster or haplotype.

5

Only Possibly Related

32/37 You share the same surname (or a variant) with another male and you mismatch by five 'points' --a 32/37 match. It is most likely that you did not 12/12 or 24/25 or 25/25 in previous Y-DNA tests. If several or many generations have passed it is possible that these two group members are related through other family members. That would require that each line had experienced separate mutations and one person would have experienced at least 2 mutations. The only way to confirm or deny is to test additional family lines and find where the mutation took place. Only by testing additional family members can you find the person in between each of you...this 'in betweener' becomes essential for you to find, and without him only the possibility of a match exists, further evidence should be pursued. If you test additional individuals you must find the person whose DNA results fall in-between the persons that are 5 apart demonstrating relatedness within this family cluster or haplotype.

6

Not Related

31/37 is too far off to be considered related, unless you can find an “in-betweener’ as for determining ‘Only Possibly Related,’ above. It is important to determine what set of results most typifies the largest number members of the group you are 'close' to matching. You may be 31/37 with an individual, but 34/37 with the center of the group, and your potential relatedness to him is through the center of the group.

Beyond 6

Not Related

30/37 You are not related and the odds greatly favor that you have not shared a common male ancestor with this person within thousands of years. You are probably even in different Haplogroups on the Phylogenetic tree of Homo Sapiens.

 

 

 

67 Marker Results

Click for full 67 marker table

Distance

Relatedness

Explanation

0

Very Tightly Related

67/67 Your perfect match means you share a common male ancestor with a person who shares your surname (or variant). Your relatedness is extremely close with the common ancestor predicted, 50% of the time, in 3 generations or less and with a 90% probability within 5 generations. Very few people achieve this close level of a match. All confidence levels are well within the time frame that surnames were adopted in Western Europe.

1-2

Tightly Related

65-66/67 You share the same surname (or a variant) with another male and you mismatch by only one or two 'points' at only one marker. It's most likely that you matched 36/37 or 37/37 on a previous Y-DNA test. Very few people achieve this close level of a match. All confidence levels are well within the time frame that surnames were adopted in Western Europe.

3-4

Related

63-64/67 You share the same surname (or a variant) with another male and you mismatch by only three or four 'points’. It's most likely that you matched 24/25, 36/37 or 37/37 on previous Y-DNA tests and your mismatch will be found within the second panel at DYS #'s 458, 459 a, 459b, 449, or within 464 a-d, or at DYS 576, 570, CDYa or CDYb in our third panel of markers. Your common ancestor is probably not extremely recent, but your mismatch is likely within the range of most well established surname lineages in Western Europe.

5-6

Related

61-62/67 You share the same surname (or a variant) with another male and you mismatch by five or six 'points'. Because of the volatility within some of the markers this is slightly tighter than being 11/12, 23/25, or 33/37, and it's most likely that you matched closely on previous Y-DNA tests. It's most likely that you matched 24/25, 36/37 or 37/37 on previous Y-DNA tests and your mismatch will be found within the second panel at DYS #'s 458, 459 a, 459b, 449, or within 464 a-d, or at DYS 576, 570, CDYa or CDYb in our third panel of markers. Your common ancestor is not very recent, but your mismatch is likely within the range of most well established surname lineages in Western Europe.

7

Probably Related

60/67 You share the same surname (or a variant) with another male and you mismatch by seven 'points'. Because of the volatility within some of the markers this is about the same as being 11/12 and it's most likely that you matched 23/25 or 24/25 or 33-34/37 on previous Y-DNA tests. If several or many generations have passed it is likely that these two lines are related through other family members. The only way to confirm is to test additional family lines and find where the mutations took place. Only by testing additional family members can you find the person in between each of you...this 'in betweener' becomes essential for you to find, and without him the possibility of a match exists, but further evidence must be pursued. If you test additional individuals you will most likely find that their DNA falls in-between the persons who are 7 apart demonstrating relatedness within this family cluster or haplotype.

8-9

Only Possibly Related

58-59/67 You share the same surname (or a variant) with another male and you mismatch by eight or nine ‘points’. It is most likely that you did not match 24-25/25 or 35-37/37 in previous Y-DNA tests. If several or many generations have passed it is possible that you are related through other family members. The only way to confirm or deny is to test additional family lines and find where the mutation took place. Only by testing additional family members can you find the person in between each of you...this 'in betweener' becomes essential for you to find, and without him only the possibility of a match exists, but further evidence should be pursued. If you test additional individuals you must find the person whose DNA results falls in-between the persons that are 8 or 9 apart demonstrating relatedness within this family cluster or haplotype.

10-11

Not Related

56-57/67 is too far off to be considered related, unless you can find an “in-betweener’ as for determining ‘Only Possibly Related,’ above. It is important to determine what set of results most typifies the largest number members of the group you are 'close' to matching. You may be 57/67 with an individual, but 61/67 with the center of the group, and your potential relatedness to him is through the center of the group.

Beyond 11

Not Related

55/67 You are not related and the odds greatly favor that you have not shared a common male ancestor with this person within thousands of years.

 

 

Interpretation of the Results

 12 Marker Results:

 

From the 12 marker results, we now have 30 groups of people who are related within themselves, but not related to anyone else in the other groups.  These groups are identified by the boxes in the genetic distance tables.  The family group number is shown across the top of the table, and the Haplogroup type is shown down the left side of the table.  The 12-marker tables are separated by the three Haplogroups represented, R1b1, R1a, and I, since there is no common ancestor between these groups within several thousands of years.  As noted above, James F Osburn and Dale Evert Osborn are the only people in the project with an E1b Haplotype so there is no genetic distance table yet shown for E1b Haplotypes.   They are not related to anyone else in the project or to each other.

 

Family Group 1 now has 11 members and 10 have a 0 genetic distance, or a perfect 12 marker match, between them.  These are all definitely related within the past few hundred years and for most the actual ancestral lines are shown in the Family Group 1 page.  One person has a genetic distance of one to the other 10. 

 

Jeffrey P Osborne and Felipe Osborne Shea have a genetic distance of 1 to most of the members in Family Group 1, and normally would be considered to be in that Family Group.  However Felipe’s subsequent 25-marker test shows that they are not related to FG1, so they have been assigned Family Group 20.  This is a case where the 25 marker test shows different results from the 12 marker test and demonstrates the better accuracy of the higher level tests.  

 

Family Group 2 consists of 4 subgroups, each consisting of 2 or 3 people who are a genetic distance of 0 to the other person in the subgroup, but are a distance of 1 or 2 to the others in the Family Group.  In this Family Group are Charles, Jerry, and Kevin with a 0 distance between them; James and Harry with a 0 distance between themselves but with a distance of 1 to everyone else in the group; Milton and Gary with a 0 distance between themselves, but 2 away from the first group; and Darrell and Charles M with a 0 distance between themselves, but distance of 1 and 2 to others in the Family Group.  However, the mutations for Charles, Milton, and Darrell are on different Alleles making the genetic distance between them a value of two.  This would normally indicate that they are probably not related, but since the mutations are on different Alleles as highlighted in the Alleles table, this is the example given above for the case where a distance of two may still mean they are related.  For Charles, the mismatch is on marker DYS 439 which is a “fast” marker.  This group is interesting in that it is not as homogeneous as the other large groups.  Out of all the people in FG2, only two, Darrell and Charles know how they are related.

 

The order of the people in Family Group 2 has been arranged to emphasize the closeness of this group to FG1.  Jeffrey and Felipe in FG20 are a “bridge” between FG1 and FG2 because they are a distance of 1 from all the others in FG1 and yet are also a distance of 1 from 5 people in FG2, Charles, Jerry, Kevin, Milton, and Gary.  These five are in turn a distance of 1 to two others in FG2, James and Harry, but are a distance of 2 from Darrell and Charles.  Unfortunately, at the present time, we do not have Jeffrey P’s ancestors and Felipe’s distant ancestors are not known so we cannot compare lines.  However, my personal speculation is that Family Groups 1, 2, and 20 share a common ancestor at some point back in early England, probably about the time surnames started being used.

 

Family Group 3 now consists of Lynn Simons alone, as her (actually her surrogate donor) genetic distance is at least two from any other person in the project.  She comes closest to matching Milton and Joseph W with a genetic distance of two, and also has an R1b haplotype.

 

Family Group 4 now has 27 people and is the largest Family Group in the project.  With the new members in this group, their results, and the additional connections to Thomas m Mary Goatley, there is more evidence that everyone in this group is related in some way to this immigrant Thomas Osborne.  Three groups now know how they are related between themselves:  A group of six, with Gerald, Nancy, Wayne, Bartley, Mark, and Daniel, now have their ancestors all the way back to John Osborn of Ashford, Kent, England, ancestor of the immigrant Thomas Osborne m Mary Goatley.  Joseph M Osborn and Gerald E Osborne know how they are related; and John P and Denver J Osborne know how they are related.  The remaining people still do not know how they connect to anyone else, but with the dna results consistently indicating that they are descendants of this Thomas, there can be only a few missing generations to find.  See the FG4 page for more details.

 

In Family Group 5 are Francis and Joseph who are father and son.  They are not related to any other person in the project.

 

All the other people with an R1b1 Haplotype are not related to anyone else in the project and therefore are assigned their own Family Group.  Each is waiting and hoping that someone else will join the project and will be shown to be related to them. 

 

Family Group 6 is a group of 11 people, all having an R1a Haplotype.  Their genetic distances are shown in the R1a table.  At the 12 marker level, 9 of these people have a genetic distance of 0 between them, and a genetic distance of 1 to the other two people in the Family Group.  All of the people in this group know how they are related except for three people.  All are believed to be descendants of the immigrant Benjamin Osborne of Baltimore/Harford Co., BD as shown on the FG6 page.

 

All of the others in the project, with the exception of James F Osburn as mentioned above, have an I Haplotype and are shown in the I Haplotype table.

 

Family Group 7 now has 6 members, all with a genetic distance of 0.  Garry had not joined our project originally, but when his tests came back, he was a perfect match to Michael on both 12 and 25 marker tests, which indicates a close common ancestor.  Because both he and Michael had signed the release agreement, each was notified of the match, and we finally made contact with each other.  Garry’s results were then listed in our project too and he became a member of our project.  This was an excellent demonstration of the benefits of signing a release.

 

Family Group 9 now has Debra O Spindle and Rhonda Ballinger.  They do not know how they are related but have a genetic distance of 0 between them.

 

Family Group 11 contains Merlyn Robb Osborn and Carlton Morris Osburn.  These two share a common ancestor, Richard Osborn, b 1612.  They are a perfect match on the 12-marker test, and a genetic distance of 1 on the 25 marker test.  Their closest genetic distance to anyone else in the project is 3 to Debra O Spindle, perhaps indicating some distant relation to her.

 

Family Group 13 is composed of Marvin A Ausburn.  This is Tony Ausburn, founder of our project, who is known to be an adopted Ausburn, but he is trying to find out more about his natural line.

 

Family Group 16 is composed of only Karma and Leo Osborn.  Karma is researching her husband and son’s line using her son’s dna.  Their closest distance to anyone else in the project is 4 to Marvin Anthony Ausburn, who is an adopted Ausburn, and not really in the Osborn/Ausburn line. By current rules this distance is too large to be considered related.

 

Family Group 18 consists of Raymond K Osborne, again a distance of 4 to the nearest person in the project and considered not related.

 

Family Group 19 consists of Richard N Osborne.  The closest other member is Larry D Osborne who is a genetic distance of 2 and usually considered not related.  He is a genetic distance of 3 from several other members of the project.

 

Family Group 20 now consists of Jeffrey P Osborne and Felipe Osborne Shea.  These two were previously thought to be members of Family Group 1 based on the 12-marker tests, but Felipe’s 25 marker test definitely shows he is not related to FG1 in spite of the 12-marker test results.  To confirm that no mistakes were made, FTDNA repeated the 12-marker tests at the same time they did the 25-marker test and the results were the same.  This is the first time in our project that the 25-marker tests have not confirmed the earlier 12-marker tests, but it is apparently not too unusual.

 

Family Group 21 consists of Lloyd W Osborn.  His genetic distance is 2 to the nearest members of the surname project, James Ausburn and Harry D Ozburn, who are presently shown in Family Group 2.  This is interesting because James and Harry are the only ones in FG2 who are a Genetic Distance of one, hence “probably related,” to everyone else in FG2.  However, by current rules, a GD of 2 means probably not related, so this indicates that Lloyd is probably not related in recent genealogical times to anyone else in the project at the present time.

 

Family Group 22 consists of Douglas E Osborne.  His genetic distance is 1 to the nearest members of the surname project, Jeffrey P Osborne and Felipe Osborne Shea, who are presently shown in Family Group 20.  Normally this would indicate “probably related”.  However, the 25- and 37-marker tests definitely show that he is not related to anyone else in the project, so he has been placed in a new Family Group 22.

 

Family Groups 23, William L Osborne; 24, Charlie Boone Osborn; 25, Christopher John Osburn; 26, David Laurence Osborne; 27 Dale Evert Osborn; 28; Robert D Osborn; 29, Aubrey Charles Osman; and 30, Michael Cordell Ozbun; each have no relationship to anyone else in the project.

 

We have several family groups with several people in each who are apparently related.  Some know how they are related to each other as shown on the family group pages, and some do not as in Family Group 4.  There are 3 family groups with two people in each one.  One is Francis and Joseph who are father and son so really count as one person.  But two family groups, 7 and 11, have two people who have discovered each other through dna testing.  The two people in Family Group 7 are closely related being a 0 genetic distance on the 25-marker test, but do not know how they are related.  The two people in Family Group 11 share a common ancestor back 11 generations.  Out of the almost 100 people tested so far, there are 26 distinct lines which are not related in recent genealogical times, may not be related in a period after surnames came into use, and indeed may not be related at all except in ancient times. 

 

Although the 12-marker test remains the basic entry level test, we now encourage people to start with at least the 25-marker test because of the increased accuracy.  Higher level tests basically narrow the probablility curve indicating the time period of the common ancestor.  More and more people are getting the higher level tests.

 

25 Marker Results:

 

Twenty Family Groups and 61 people are now represented in the 25 marker results.

 

 

37 Marker Results:

 

Forty-three people from 17 Family Groups have now been tested with 37 markers, but only Family groups 1, 2, 4, 6, 7, 9, and 11 have more than one person tested. 

 

 

67 Marker Results:

 

At the present time, 9 people representing 5 Family Groups have had results returned for the 67 marker test.  Four people in Family Group 4 all have a genetic distance of 2 between them which indicates a recent common ancestor.  Marvin A “Tony” Ausburn has also had a 67 marker test, but there is no one in his Family Group to compare to.

 

 

FTDNA Haplotype Estimates.

 

This is the comment that FTDNA now uses with their Haplogroup determinations:

* Haplogroups in green have been confirmed by SNP testing. Haplogroups in red have been predicted by Family Tree DNA based on unambiguous results in the individual's personal page. Please note that for any predicted results we see no reason for ordering a SNP test to confirm the Haplogroup.  If a ‘–‘ (dash)  is in the HAPLO field then we feel that the comparative results are not clear and unambiguous and if the kit holder wants to know their SNP with 100% confidence they may consider ordering a SNP confirmation test.”

 

HOWEVER, FTDNA still makes an estimate of each person’s Haplogroup based on the test results, even for those that are shown with a ‘-‘ (dash) in the Allele table HAPLO field.   In the tables shown on this web site, I have replaced the dash with that estimated Haplogroup, shown in orange with parentheses to indicate it is not certain, in order to give some indication of the Haplogroup for each person.  All of the project members fall into the Haplogroups, R1b, R1a, I, and E1b, which are the most common values found by FTDNA in all their tests. Lee’s Haplogroup has been confirmed by a SNP test to be R1a and is shown in green.  Based on his results, I have indicated that everyone else in that Subgroup is also R1a.  

 

FTDNA’s description of these groups is repeated below for convenience and Migration Maps are shown for each Haplotype.  These maps are accessable through each persons personal web page on FTDNA.

 

FTDNA Haplogroup Descriptions.

 

The following Haplogroup Descriptions are from the FamilyTreeDNA.com website which was the testing company used to determine the nearest Haplogroup assignment based on the individual's haplotype results from the Y-DNA test. These verbatim Haplogroup Descriptions and/or excerpts are copyrighted by FamilyTreeDNA.com and all rights to these descriptions are claimed by FamilyTreeDNA.com. These descriptions have been printed here with the permission of FamilyTreeDNA.com. These descriptions cannot be used elsewhere without the written permission of FamilyTreeDNA.com.

 

R1a  The R1a lineage is believed to have originated in the Eurasian Steppes north of the Black and Caspian Seas. This lineage is believed to have originated in a population of the Kurgan culture, known for the domestication of the horse (approximately 3000 B.C.E.). These people were also believed to be the first speakers of the Indo-European language group. This lineage is currently found in central and western Asia, India, and in Slavic populations of Eastern Europe.  The migration map for this haplogroup is shown below:

 

 

R1b  Haplogroup R1b is the most common haplogroup in European populations. It is believed to have expanded throughout Europe as humans re-colonized after the last glacial maximum 10-12 thousand years ago. This lineage is also the haplogroup containing the Atlantic modal haplotype.  The migration map for this haplogroup is shown below:

 

 

I   The I, I1, and I1a lineages are nearly completely restricted to northwestern Europe. These would most likely have been common within Viking populations. One lineage of this group extends down into central Europe. There is a dna project at FTDNA that is dedicated to the study of yDNA Haplogroup I Subclade I1a.  More information on this project can be found at this web site:

http://www.familytreedna.com/(phwblr55cnbpn145atzbw555)/public/yDNA_I1a/index.aspx?fixed_columns=on

The migration map for this haplogroup is shown below:

 

 

E1b  This haplogroup is believed to have evolved in the Middle East. It expanded into the Mediterranean during the Pleistocene Neolithic expansion. It is currently distributed around the Mediterranean, southern Europe, and in north and east Africa.  The migration map is shown below:

 

 

The different Haplogroups explain why there are such large genetic distances between certain groups.  For more on Haplogroups, see   http://www.ivey-ivie-ivy.org/dna/haplogroups.htm   and http://freepages.genealogy.rootsweb.com/~dgarvey/DNA/markers.htm   and the references linked there.  For a discussion of where these Haplogroups are found and their possible origins, see  http://www.davidkfaux.org/shetlandislandsresstudies3.html.

 

 


Actual Allele Values Reported by FTDNA

 

The two Alleles Tables, for 1 to 37 markers, and 38 to 67 markers, list the actual Allele values reported by FTDNA.  The two tables have been separated to prevent them from being so wide and difficult to read.  Individuals are grouped according to their Family Groups, and the linked Family Group pages tell more about the ancestors of the individuals who have been tested.  By comparing the known ancestors of those individuals who appear to be related, we hope that their common ancestors can be determined, and any new or potential members can determine if they might belong to a known subgroup.

 

 


 
Click here for the 1 to 37 marker allele table


Click here for the 38 to 67 marker allele table

 


FTDNA Comments for above tables:  “DYS 19 is also known as DYS 394.

 

It is obvious from our observation of 1000's of samples that some markers change or mutate at a faster rate than others. While that actual 'faster rate' has not yet been definitively calculated, not all markers should be treated the same for evaluation purposes.

The markers in red have shown a faster mutation rate then the average, and therefore these markers are very helpful at splitting lineages into sub sets, or branches, within your family tree.

Explained another way, if you match exactly on all of the markers except for one or a few of the markers we have determined mutate more quickly, then despite the mutation this mismatch only slightly decreases the probability of two people in your surname group who match 11/12 or even 23/25 of not sharing a recent common ancestor.

 

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This page was last updated on Feb 14, 2009