To quote from familytreedna.com,
which did this testing:
Genetic Distance
When comparing peoples samples
in our system we show individuals who are closely matched, but
not identically matched, as being different by what the Anthropologists
call genetic distance.
If two people were identical in
all markers except they are off in one marker by 1 point, the
genetic distance would be 1. If they were off at 2 different
markers by 1 point in each marker, then the genetic distance
of those two samples would be 2. If they were off by 2 points
at one marker and 1 point in a second marker, then the genetic
distance would be 3. This is called the Stepwise Model of calculating
genetic distance for shallow time depths (i.e. Genealogy not
Anthropology).
If you and another person match
in all 12 loci -- If you share the same surname or variant, this
means that there is a 99% likelihood that you share a common
ancestor in a genealogical time frame. If you match another person
without the same surname or variant, you still probably share
a common ancestor, but this ancestor most likely lived in the
time before surnames were adopted.
It is obvious from our observation
of 10's of 1000's of samples that some markers change or mutate
at a faster rate than others. Therefore 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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