A large data resource of genomic copy number variation across neurodevelopmental disorders.

NPJ Genom Med · 2019 · PMC6779875 · PMID 31602316

Europe PMC DOI

hedged sentence

0.0800

closest p · 1.6× alpha

0.0800

boldest claim

The sentences

nearly significantp = 0.08so close (0.05 < p ≤ 0.1)

We found a nearly significant excess in cases over controls of deletions in protein-coding genes ( p = 0.08; false discovery rate (FDR) = 0.21), but not for lncRNAs ( p > 0.1).

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