The clinical impact of copy number variants in inherited bone marrow failure syndromes.

NPJ Genom Med · 2017 · PMC5498150 · PMID 28690869

Europe PMC DOI

hedged sentence

0.0700

closest p · 1.4× alpha

0.0700

boldest claim

The sentences

did not reach statistical significancep = 0.07so close (0.05 < p ≤ 0.1)

A trend was seen towards more cases showing “extensive non-hematological organ system involvement” for the specific syndromes with CNVs (75%) compared to those without (39%) but the difference in incidence did not reach statistical significance ( p = 0.07).

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