Barely Significant
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Copy number variations in the genome of the Qatari population.

BMC Genomics · 2015 · PMC4618522 · PMID 26490036

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highly significantno p-value reported
There was a highly significant improvement of up to 250 % for all CNVs and almost 1.5 times that (367 %) for genic CNVs at r 2 = 1 (Fig. 3b and Additional file 1 : Table S3).

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