Distribution of sequence mismatches to array probe sets.

The first column shows the gene and sample analyzed (+D: most depressed; −D: least depressed, All: +D, −D and controls). The next four columns indicate the number of samples, sites that are polymorphic using a relaxed criterion* (SNPs supported by one sequenced strand), sites that are polymorphic using a strict criterion** (SNPs supported by the two sequenced strands), and the number of fixed nucleotide differences to each microarray probe set. The number of non-synonymous changes out of the total is indicated in parenthesis.