Barely Significant
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Assessment of copy number variations in the brain genome of schizophrenia patients.

Mol Cytogenet · 2015 · PMC4487564 · PMID 26136833

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highly significantno p-value reported
Conclusion The present CGH analysis lists the potential candidate regions of somatic CNVs associated with schizophrenia, although most of those exhibited the modest but highly significant alterations in brain genome doses.

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