Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis.

Hum Mol Genet · 2011 · PMC3024044 · PMID 21131291

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nominally significantno p-value reported

However, in a combined analysis of both family-based samples, three CNVRs presented at least nominally significant CNVR-adjusted one-sided P -values (≤0.025; Table 2 ).

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