Originally posted by Chris
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Hypervariable region 1:
T16126C - 12.6%
A16163G - 1.63%
C16186T - 1.51%
16188T - 0.633%
16189C - 27.3%
C16294T - 10.4%
T16519C - 61.2%
Putting these sequence variations into HaploGrep does indeed produce T1a1 as the top suggestion. But there are four discrepancies - one sequence variation expected but not present, and three present but not expected.
I think it's clear that the result of this indirect procedure - of using a partial sequence from the "shawl" to obtain a match in a database, and then finding the haplogroup of the matching sequence - will be very sensitive to how much of the "shawl" DNA was sequenced.
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