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Chunk #8 — Materials And Methods — Genotyping of the discovery dataset

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A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.
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Samples that passed the above exclusion criteria were genotyped using Illumina's Human 1Mv1 Beadchip, containing 1,072,820 SNPs (of those 258,665 loci are in reported and new CNV regions). The samples have been processed according to Illumina Procedures for processing of the Infinium II ® assay.