-this page will always be under construction-

Brink Genealogy Project

Y-DNA Test Results (12-markers)
for participants in this project, et. al.
note-The more alleles that match, the closer the relationship.

UPDATED 21 JULY 2010

row identification test
date
Haplo-
group
393 390 19(394) 391 385a 385b 426 388 439 389-1 392 389-2
1 001 Brink 2006 R1b1 14 25 15 10 11 14 12 12 12 14 13 30
2 002 Brink 2006 R1b1 13 24 14 10 11 14 12 12 12 14 13 30
3 003 Brinck 2008 R1a 13 25 16 10 11 14 12 12 11 13 11 29
4 004 Brink 2008 Q1a3 13 24 13 10 15 18 12 12 11 12 16 29
5 005 Brink 2008 G 12 22 15 10 14 15 11 13 12 12 11 29
6 006 Brink 2009 R1b1b2a 12 23 14 11 10 14 12 12 12 13 12 30
7 007 Brink 2010   13 24 14 11 11 14 12 12 12 13 13 29
8 oth-F Brink unk E3b 13 24 13 10 16 18 11 12 14 13 11 30
9 oth-SA Brink unk   13 24 15 10 11 14 12 12 12 13 13 30
10 oth-SP Brink unk   13 24 15 10 11 14 12 12 12 13 13 30
11 oth-SM Brinks unk   13 23 14 11 11 14 12 12 12 13 13 30

definitions are given farther down the page

also see the DNA Interpretation page

note:  Participant 001 is believed to be a direct Y-chromosome descendant of
Lambert Huybertse (Brink), a man born in the early 1600's in The Netherlands and
who is believed to be the Y-chromosome ancestor of all of the early Brinks in the
North American Colonies and early states.

Participant 002 has an unknown European lineage, but is known to be a descendant of Washington Perry Brink, the founder of Brink's Express, now the Brinks Company.  The first three markers differ between participants 001 and 002, although the other nine markers are the same.

FTDNA classified his haplogroup as H1b, a common one in Europe.  More results
should allow a finer analysis of where the Brink lines came from.

TERMINOLOGY DEFINITIONS
these are non-technical definitions, as much as possible

locus

A location on a chromosome.

allele

This refers directly to the DNA coding -- specifically, in genetic genealogy, this is usually a set of STRs (short tandem repeats), short sequences of letters (base pairs) that are repeated 10-100 times.  For example, the letter sequence GATA might be repeated 10 times.  That allele would have the pattern:

GATAGATAGATAGATAGATAGATAGATAGATAGATAGATA

This means that when the chromosome is "sequenced" the location (locus) for this sequence would be identified as having 10 repeats. A mutation at this locus might result in an additional GATA to be inserted thus making the STR count to increase to 11. 

The allele numbers in the table above refers to the numbers of repeats (STRs) at the tested locations.  It is these repeats that are used to determine closeness of relationship.

haplogroup

Haplogroups are constructed through a mathematical comparison of the DNA data from thousands of individuals.  Individuals with many identical alleles would likely be classified in the same haplogroup. Y-DNA haplogroup R1b is strongly associated with Western Europe.  There has been a great deal of research on the distribution and migration of population haplogroups around the world.

markers

Alleles/mutations that are used as tools by researchers to identify something, such as closeness of relation or inherited diseases.