CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1.

Hum Mol Genet · 2014 · PMC3929090 · PMID 24163246

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nominally significantno p-value reported

In the replication data, CNVs of the same type (deletions or duplications) at 20 of the 33 loci were more common among cases ( Supplementary Material, Table S5 ) but only one (16p12.1) was nominally significant (without multiple-testing correction).

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