Barely Significant
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Genome-wide copy number variation association study in anorexia nervosa.

Mol Psychiatry · 2025 · PMC12014356 · PMID 39533101

Europe PMCDOI
1
hedged sentence
0.0210
closest p · 0.4× alpha
0.0210
boldest claim

The sentences

nominally significantP = 0.021actually significant
The first ancestry PC showed a nominally significant association ( P = 0.021) to small CNV burden (autosomal <100 kb CNV burden) and was included as a covariate.

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