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Accession: PRJEB37584 ID: 623833

Homo sapiens (human)

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

See Genome Information for Homo sapiens
Genome-wide genotyping analysis identified copy number variations in cranial meningiomas in Chinese patients, and demonstrated diverse CNV burdens among individuals with diverse clinical features.
AccessionPRJEB37584
ScopeMonoisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 8-Apr-2020
European Bioinformatics Institute
Project Data:
Resource NameNumber
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BioSample1
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    Homo sapiens
    High copy number variation burdens in cranial meningiomas from patients with diverse clinical phenotypes characterized by hot genomic structure changes
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