The clinical significance of small copy number variants in neurodevelopmental disorders.

J Med Genet · 2014 · PMC4173859 · PMID 25106414

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did not reach statistical significanceno p-value reported

7 Accordingly, 12 of our 41 confirmed rare small deletions (29%) were pathogenic, but only 2 of 17 confirmed rare duplications (12%) were categorised as such, but the difference did not reach statistical significance.

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