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Accession: PRJNA674608 ID: 674608

Homo sapiens (human)

Germline copy number variations and breast cancer risk

See Genome Information for Homo sapiens
The current sudy aimed to evaluate the contribution of germline CNVs to hereditary breast cancer risk in Tunisian patients who were negative for pathogenic mutations in known breast cancer susceptibility genes. More...
AccessionPRJNA674608
Data TypeVariation
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 4-Nov-2020
Institut Pasteur de Tunis
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Variation (dbVar)281

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    Germline copy number variations and breast cancer risk
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