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Copy number variants in autism spectrum disorders

ABSTRACT: Our cohort comprised 40 non-syndromic ASD children.We conducted genome wide analysis using Affymetrix Cytoscan-HD microchips. We identified pathogenic CNVs in 7 patients (17.5%), other variant classified as variants of uncertain significance (VUS) or benign.

ORGANISM(S): Homo sapiens

PROVIDER: GSE270110 | GEO | 2025/04/22

REPOSITORIES: GEO

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