Germline copy number variants and endometrial cancer risk

Known risk loci for endometrial cancer explain approximately one third of familial endometrial cancer. However, the association of germline copy number variants (CNVs) with endometrial cancer risk remains relatively unknown. We conducted a genome-wide analysis of rare CNVs overlapping gene regions i...

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Bibliographic Details
Main Authors: Stylianou, CE, Wiggins, GAR, Lau, VL, Dennis, J, Shelling, AN, Wilson, M, Sykes, P, Amant, F, Annibali, D, De Wispelaere, W, Easton, DF, Fasching, PA, Glubb, DM, Goode, EL, Lambrechts, D, Pharoah, PDP, Scott, RJ, Tham, E, Tomlinson, I, Bolla, MK, Couch, FJ, Czene, K, Dörk, T, Dunning, AM
Format: Journal article
Language:English
Published: Springer 2024