Extended Data Fig. 3: Consistency of effect sizes of pLoF CNV and SNP/indel variants across gene-trait associations. | Nature Genetics

Extended Data Fig. 3: Consistency of effect sizes of pLoF CNV and SNP/indel variants across gene-trait associations.

From: Protein-altering variants at copy number-variable regions influence diverse human phenotypes

Extended Data Fig. 3

Data are shown for all associations discovered only upon considering pLoF CNVs (i.e, not reaching significance in SNP/indel-only burden tests). The top plot is a merge across all traits, and the bottom plots show each phenotype category separately. Error bars are 95% confidence intervals. Sample sizes are reported in Supplementary Data 1.

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