Numbers | Microsatellites | Chromosomal locations | Numbers of detectable alleles (frequencies of the most common allele in Causasians) | Genotypes | |
1 | D8S1179 | 8 | 12 | (13:35.52%) | 13-14 |
2 | D21S11 | 21q11.2-q21 | 24 | (30:25.21%) | 27-29 |
3 | D7S820 | 7q11.21-22 | 10 | (10:27.22%) | 9-10 |
4 | CSF1PO | 5q33.3-34 | 10 | (12:32.81%) | 11 |
5 | D3S1358 | 3p | 8 | (15:25.35%) | 14-16 |
6 | THO1 | 11p15.5 | 10 | (9.3:29.08%) | 8-9.3 |
7 | D13S317 | 13q22-31 | 8 | (12:30.80%) | 13 |
8 | D16S539 | 16q24-qter | 8 | (12:30.23%) | 11-12 |
9 | D2S1338 | 2q35-37.1 | 14 | (19:22.76%) | 17-23 |
10 | D19S433 | 19q12-13.1 | 15 | (14:34.10%) | 13 |
11 | vWA | 12p12-pter | 14 | (17:24.50%) | 16-18 |
12 | TPOX | 2p13-pter | 8 | (8:53.30%) | 8 |
13 | D18S51 | 18q21.3 | 22 | (14:16.76%) | 11-16 |
14 | D5S818 | 5q21-31 | 10 | (11:39.26%) | 11 |
15 | FGA | 4q28 | 28 | (24:13.75%) | 23-24 |
Amelogenin | Y | XY |