Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers.

Commun Biol · 2022 · PMC9537519 · PMID 36203093

Europe PMC DOI

hedged sentence

0.0550

closest p · 1.1× alpha

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boldest claim

The sentences

did not reach statistical significancep = 5.5 × 10 −2so close (0.05 < p ≤ 0.1)

3g , Supplementary Data 11 ) in MCF7–BRCA1 +/− cells, the reduction in the number of foci caused by the siSULT1A1 transfection did not reach statistical significance ( F (1, 8) = 5.02, p = 5.5 × 10 −2 ).

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