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High copy number variation burdens in cranial meningiomas from patients with diverse clinical phenotypes characterized by hot genomic structure changes

ABSTRACT: Meningiomas, as the most common primary tumor of the central nervous system, are known to harbor genomic aberrations that associate with clinical phenotypes. Here we performed genome-wide genotyping for cranial meningiomas in 383 Chinese patients and identified 9,821 copy number variations (CNVs).

ORGANISM(S): Homo sapiens

PROVIDER: GSE147673 | GEO | 2020/03/28

REPOSITORIES: GEO

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