Table 4.

Number of overlapping SNP AIMs selected by different platforms (HapMap, Affymetrix, Illumina, and AIMs).

Chr	H<->A	H<->I	H<->S	A <->I	A<->S	I<->S	H<->A<->I	H<-> A<>S	H<->I <->S	A<->I <->S	All
1	1923	0	107	0	5	0	0	1	0	0	0
2	2180	0	114	0	7	0	0	5	0	0	0
3	1983	0	88	0	1	0	0	1	0	0	0
4	1433	0	58	0	6	0	0	3	0	0	0
5	1590	0	71	0	7	0	0	4	0	0	0
6	1836	0	105	0	8	0	0	7	0	0	0
7	1240	0	55	0	2	0	0	2	0	0	0
8	1546	0	61	0	5	0	0	4	0	0	0
9	1073	0	63	0	2	0	0	2	0	0	0
10	1275	0	69	0	5	0	0	2	0	0	0
11	1167	0	67	0	2	0	0	1	0	0	0
12	1071	0	67	0	6	0	0	5	0	0	0
13	1073	0	38	0	1	0	0	1	0	0	0
14	760	0	46	0	2	0	0	2	0	0	0
15	863	0	45	0	2	0	0	2	0	0	0
16	824	0	52	0	4	0	0	3	0	0	0
17	694	0	56	0	2	0	0	2	0	0	0
18	883	0	55	0	5	0	0	3	0	0	0
19	244	0	48	0	1	0	0	1	0	0	0
20	863	0	47	0	3	0	0	3	0	0	0
21	431	0	31	0	6	0	0	5	0	0	0
22	361	0	41	0	5	0	0	1	0	0	0
X	1075	0	95	0	7	0	0	5	0	0	0

Chr = chromosome, H = HapMap, A = Affymerix, I = Illumina, and S = AIMs identified by Smith et al. (2004)