Barely Significant
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CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank.

Cell Genom · 2022 · PMC9903682 · PMID 36779085

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highly significantno p-value reported
45 , 46 Recent large-scale CNV association testing using datasets such as the UK Biobank have found some highly significant loci in relation to certain human traits, 47 and previous studies focused on cognitive traits such as schizophrenia 48 and autism 49 have demonstrated the utility of SNP arrays to search for novel CNV associations.

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