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Author Topic: Last news from DYS464  (Read 811 times)
Maliclavelli
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« on: August 07, 2010, 12:11:35 PM »

Should I thank my friend Ricardo Costa de Oliveira for this Brazilian science?
The paper "Worldwide diversity of the Y-chromosome tetra-local microsatellite
DYS464" by F.S.G. Kehdy and S.D.J. Pena (Genetics and Molecular research, 9:
1525-1534 (2010)), would seem having resolved the long inquiry about my origin:
my values (and those of my relatives so far known: Giancarlo Tognoni and the
Anonymous Brazilian) are: 14-14-16-17 and the paper says that they are present
in Middle East (0.012) and East Asia (0.005). Not having "olhos puxados", my
origin would be in Middle East, then I am an Etruscan from Asia Minor or a
Jew, having also a 23% of Ashkenazi ancestry on my autosomes.

But my values are probably the mutations from the modal of my haplogroup (R1b1b2a):
14-15-16-18 by two mutations: DYS464b from 15 to 14 and DYS464d from 18 to 17,
like others are 15-15-16-17 (many Jewish clades), 15-15-17-17 the European par
excellence WAMH etc. etc.

Should I thank my friend Ricardo Costa de Oliveira?
« Last Edit: August 07, 2010, 12:57:39 PM by Maliclavelli » Logged

Maliclavelli


YDNA: R-S12460


MtDNA: K1a1b1e

Maliclavelli
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« Reply #1 on: August 08, 2010, 01:03:18 AM »

Of course I don't think that my DYS464 has had only two mutations from the modal
of my haplogroup, being also a relatively fast mutating marker and whose setting
of the single marker is unknown, but that this is the result of numerous mutations
around the modal of each marker. Practically these configuration is the modal of each clade that mutates frequently and continually.
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Maliclavelli


YDNA: R-S12460


MtDNA: K1a1b1e

Kiwi
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« Reply #2 on: November 03, 2010, 08:13:11 PM »

My variatons on these are
15 15 16 17 is there any consensus as to where and when this variation occurs most frequently
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Colin
Maliclavelli
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« Reply #3 on: November 04, 2010, 02:46:21 AM »

These values are very common in R1b1b2 (mostly the most recent subclades), having had two mutations: DYS464a from 14 to 15 and DYS464d from 18 to 17.
This of course on average, excluding recurrent mutations.
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Maliclavelli


YDNA: R-S12460


MtDNA: K1a1b1e

OConnor
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« Reply #4 on: November 08, 2010, 08:48:53 PM »

and there is the 464x test.

I have the L21 model CCCG
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R1b1a2a1a1b4


R-DF13**(L21>DF13)
M42+, M45+, M526+, M74+, M89+, M9+, M94+, P108+, P128+, P131+, P132+, P133+, P134+, P135+, P136+, P138+, P139+, P14+, P140+, P141+, P143+, P145+, P146+, P148+, P149+, P151+, P157+, P158+, P159+, P160+, P161+, P163+, P166+, P187+, P207+, P224+, P226+, P228+, P229+, P230+, P231+, P232+, P233+, P234+, P235+, P236+, P237+, P238+, P239+, P242+, P243+, P244+, P245+, P280+, P281+, P282+, P283+, P284+, P285+, P286+, P294+, P295+, P297+, P305+, P310+, P311+, P312+, P316+, M173+, M269+, M343+, P312+, L21+, DF13+, M207+, P25+, L11+, L138+, L141+, L15+, L150+, L16+, L23+, L51+, L52+, M168+, M173+, M207+, M213+, M269+, M294+, M299+, M306+, M343+, P69+, P9.1+, P97+, PK1+, SRY10831.1+, L21+, L226-, M37-, M222-, L96-, L193-, L144-, P66-, SRY2627-, M222-, DF49-, L371-, DF41-, L513-, L555-, L1335-, L1406-, Z251-, L526-, L130-, L144-, L159.2-, L192.1-, L193-, L195-, L96-, DF21-, Z255-, DF23-, DF1-, Z253-, M37-, M65-, M73-, M18-, M126-, M153-, M160-, P66-

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