(this page will revised as more information and test results are received)

Brink Genealogy Project

Interpretation of the Y-DNA Test Results
for participants in this project, et al.

UPDATED 7 November 2008

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 oth-F Brink unk E3b 13 24 13 10 16 18 11 12 14 13 11 30
7 oth-SA Brink unk   13 24 15 10 11 14 12 12 12 13 13 30
8 oth-SP Brink unk   13 24 15 10 11 14 12 12 12 13 13 30
9 oth-SM Brinks unk   13 23 14 11 11 14 12 12 12 13 13 30

It is too early for many lineage comparisons -- more data are needed.  
The preliminary conclusion is that this is a very diverse group.  See the comparison table given
below for comparisons with the Super Western Atlantic Modal Haplotype.

About Haplogroup R1b
and the "Super Western Atlantic Modal Haplotype"
Some of this information is from articles written by Dr. Whit Athey. 

Our comparisons with the Super Western Atlantic Modal Haplotype (SWAMH), etc.
the information is presented for only the first 12 markers, red represents a mismatch

row

identification

test
date

Haplo-
group

SWAMH
match

393

390

19(394)

391

385a

385b

426

388

439

389-1

392

389-2

1

SWAMH-modal

n/a

R1b

n/a

13

24

14

11

11

14

12

12

12

13

13

29

2

001 Brink

2006

R1b1

6/12

14

25

15

10

11

14

12

12

12

14

13

30

3

002 Brink

2006

R1b1

9/12

13

24

14

10

11

14

12

12

12

14

13

30

4

003 Brinck

2008

R1a

7/12

13

25

16

10

11

14

12

12

11

13

11

29

5

oth-F Brink

unk

E3b

4/12

13

24

13

10

16

18

11

12

14

13

11

30

6

oth-SA Brink

unk

 prob R1b?

9/12

13

24

15

10

11

14

12

12

12

13

13

30

7

oth-SP Brink

unk

 prob R1b?

9/12

13

24

15

10

11

14

12

12

12

13

13

30

8

oth-SM Brinks

unk

 prob R1b?

10/12

13

23

14

11

11

14

12

12

12

13

13

30

The people listed in rows 3 and 6-7 had the closest matches to the SWAMH, although FTDNA classified the
Y-DNA given in row 2 as R1b1. 

The table below gives only those matching at least 9/12 of the SWAMH.

row

identification

test
date

Haplo-
group

SWAMH
match

393

390

19(394)

391

385a

385b

426

388

439

389-1

392

389-2

1

SWAMH-modal

n/a

R1b

n/a

13

24

14

11

11

14

12

12

12

13

13

29

2

                               

3

002 Brink

2006

R1b1

9/12

13

24

14

10

11

14

12

12

12

14

13

30

4

                               

5

                               

6

oth-SA Brink

unk

 prob R1b?

9/12

13

24

15

10

11

14

12

12

12

13

13

30

7

oth-SP Brink

unk

 prob R1b?

9/12

13

24

15

10

11

14

12

12

12

13

13

30

8

oth-SM Brinks

unk

 prob R1b?

10/12

13

23

14

11

11

14

12

12

12

13

13

30

 

A Deeper Origins Look at Haplogroup R1b (from Dr. David Faux)

The research literature provides the following explanation of the origins of the R1b haplogroup.  It is believed that during the Last Glacial Maximum the people bearing the R1b haplogroup over wintered in Iberia, and after the glacial retreat about 12,000 years before present, began a migration to the north in large numbers, and to the east in declining numbers (although probably arriving in Spain from the east 30,000 years ago among the paleolithic or "old stone age" peoples considered to be aboriginal to Europe).  It is believed that everyone who is R1b is a descendant in the male line from an individual known as "the patriarch" since his descendants account for over 40% of all the chromosomes of Europe.  This haplogroup is characteristic of the Basques whose language is probably that of the first R1b, and who are genetically the closest to the original R1b population (which probably amounted to only a few thousand individuals). 

http://www.davidkfaux.org/shetlandhaplogroupR1b 

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.