Chunk #2 — Online Methods — Cohort information — WTCCC2 UK controls

Source

Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.

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Publicly available Affymetrix Human SNP Array 6.0 was available for 6,000 individuals (3,000 from the 1958 British Birth Cohort and 3,000 from the UK Blood Service Collection) recruited for the Wellcome Trust Case Control Consortium 2 (see URLs).