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Author Topic: On the origin of mtDNA N1b  (Read 559 times)
Maliclavelli
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« on: June 08, 2010, 12:17:58 PM »
Mitosearch E7H2T (Vella from Marianopoli, Sicily) matches closely an Egyptian and two Middle Easterners, but the last two lack 16075C and 16286R and the Egyptian lacks 16286R.

How long it takes that an hetheroplasmy is fixed? Which is more ancient among these four mitochondrial?
Of course it would be interesting an FGS. Unfortunately they all are tested by SMGF.

P.S. 16286R has been found in L1c1, then it has had many time to settle.
« Last Edit: June 08, 2010, 01:07:33 PM by Maliclavelli » Logged

Maliclavelli


YDNA: R-Z2105+ L277- L584-


MtDNA: K1a1b1e

Maliclavelli
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Posts: 1949
« Reply #1 on: June 08, 2010, 01:06:02 PM »
It is probably worth noting that the same hetheroplasmy in hg. N1b was happened
in 16176C, causing the two different clades 16176G and 16176A.
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Maliclavelli


YDNA: R-Z2105+ L277- L584-


MtDNA: K1a1b1e

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