Barely Significant
← all excerpts

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations.

Nat Commun · 2020 · PMC6959272 · PMID 31937769

Europe PMCDOI
1
hedged sentence
0.0500
closest p · 1.0× alpha
0.0500
boldest claim

The sentences

nominally significantP < 0.05actually significant
To determine CNV enrichment, we only considered loci that were nominally significant between the comparative groups ( P < 0.05).

also in 7,732 other papers

Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.