About
the Project
Welcome to the Matlack/Matlick/Matlock/Medlock Y-DNA Project. Broadly, our goal
is to determine which lineages
are
related to each other. We hope this project will provide the clues and extra
evidence needed to make
breakthroughs in extending lineages that have stumped genealogists for many
decades and in connecting lineages
not
previously known to be related.
The
Administrators
Sam
Medlock (swmed@juno.com)
Terry
Gladfelter (carlg0139@aol.com)
Brenda
Avila (Ba044@aol.com)
Click
here to contact FTDNA to order your
kit or email one of the Administrators above. Be sure and let FTDNA that
you want
to join the Medlock group to get the rates posted below:
For
initial tests the costs are as follows:
| 12-marker test |
$99 |
| 25-marker test |
$124 |
| 37-marker test |
$149 |
| 67-marker test |
$248 |
The costs for upgrades are listed below:
| 12 to 25 |
$49 |
| 12 to 37 |
$99 |
| 12 to 67 |
$189 |
| 25 to 37 |
$49 |
| 25 to 67 |
$148 |
| 37 to 67 |
$99 |
Note: Keep in mind these
facts when ordering your test:
According to FTDNA, when testing
with 25 markers and if your a 25/25 match, it indicates:
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.
Updating this to a 37 marker test, and
matching 37/37 markers it indicates:
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
Doing the 67 Marker test, and matching
67/67 can close in a big gap:
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
There is
a General fund which is a feature that Family Tree DNA offers. It allows members
to donate money for other
potential
member's test. The money is used at the Group Administrator's discretion. If
interested, contact one of
the
administrators for further information, or call FTDNA at
(713) 868-1438
Test Results as
a whole.
Test
Results and Analysis
At this
time our project is supporting 6 Haplogroups. J2, E1b1b1, R1b1b2, I1,I2a and
12b1. Haplogroups are one tool
used in
splitting up groups. Having a different Haplogroups from another means that you
are unrelated. To view these
different
Groups and lineages click on the Haplogroup your interested in:
J2..1 member
The J2
lineage originated in the northern portion of the Fertile Crescent where it
later spread throughout
central
Asia, the Mediterranean, and south into India. As with other populations with
Mediterranean ancestry
this
lineage is found within Jewish populations.
Research note: Many people new to Genetic Genealogy think the J2 haplogroup is
synonymous with having male
Jewish
ancestry. One should note that having a J2 haplogroup assignment does not
necessarily indicate Jewish
ancestry.
The J2 haplogroup is far more ancient than the Jewish religion and is found in
many lines with
Mediterranean region ancient ancestry. Another relatively more recent mode for
J2's entry into some parts of
Europe
from the Mediterranean areas could have been the Roman Legions and Roman
settlements.
(http://www.kerchner.com/haplogroups-ydna.htm)
E1b1b1..8 members
According
to the International Society of Genetic Genealogy (ISOGG) and National
Geographic's
Genographic Project,
E1b1b1
may have arisen instead in the Near East or the
Middle East and then expanded into the
Mediterranean with the
spread of
agriculture.All major sub-branches of E1b1b1 are thought to have originated in
the same general area
as the
parent clade: in North Africa, the
Horn of Africa, or the Near
East. Underhill (2002) believes that the
structure
and
regional pattern of E-M35 sub-clades potentially give "reagents with which to
infer specific episodes of population
histories
associated with the Neolithic agricultural
expansion".
R1b1b2.. 40 members
The I Group...3 members
I1..1
member
The group displays a very clear
frequency gradient, with a peak of approximately 40 percent
among the populations of
western Finland and more than 50
percent in the province of Satakunta,around 35 percent in
southern Norway,
southwestern Sweden especially on the
island of Gotland, and Denmark, with rapidly decreasing
frequencies toward the
edges of the historically Germanic
sphere of influence. (http://en.wikipedia.org/wiki/I1a)
I2a..1
member
Haplogroup I2a appears to have originated in the Balkans, perhaps
from a glacial refugium there; I2a is very common in
Croatia
and Bosnia today and decreases in frequency across Eastern Europe. A rare
offshoot branch of I2a is also found
further
West, including in the British Isles. Another subgroup of I2a
is by far the most common lineage in Sardinia, but
it is
also found at low frequencies in France and Spain (http://www.ethnoancestry.com/I1b1.html)
I21b..1
member
The
distributions of Haplogroup I1 and Haplogroup I2b1 seem to correlate fairly well
with the extent of historical influence
of
Germanic peoples. Haplogroup I2b1 has been found in
over 4% of the population only in Germany, the
Netherlands, Belgium,
Denmark, England (not
including Wales or Cornwall),
Scotland, and the southern tips of
Sweden and Norway in
Northwest Europe;
the
provinces of Normandy, Maine,
Anjou, and Perche in
northwestern France; the province of
Provence in southeastern France;
the
regions of Tuscany, Umbria,
and Latium in Italy;
and Moldavia and the area around Russia's
Ryazan Oblast and Republic of
Mordovia in Eastern Europe (http://en.wikipedia.org/wiki/I1b)
