학술논문
Rare germline copy number variants (CNVs) and breast cancer risk
Document Type
article
Author
Dennis, Joe; Tyrer, Jonathan P; Walker, Logan C; Michailidou, Kyriaki; Dorling, Leila; Bolla, Manjeet K; Wang, Qin; Ahearn, Thomas U; Andrulis, Irene L; Anton-Culver, Hoda; Antonenkova, Natalia N; Arndt, Volker; Aronson, Kristan J; Freeman, Laura E Beane; Beckmann, Matthias W; Behrens, Sabine; Benitez, Javier; Bermisheva, Marina; Bogdanova, Natalia V; Bojesen, Stig E; Brenner, Hermann; Castelao, Jose E; Chang-Claude, Jenny; Chenevix-Trench, Georgia; Clarke, Christine L; Collée, J Margriet; Couch, Fergus J; Cox, Angela; Cross, Simon S; Czene, Kamila; Devilee, Peter; Dörk, Thilo; Dossus, Laure; Eliassen, A Heather; Eriksson, Mikael; Evans, D Gareth; Fasching, Peter A; Figueroa, Jonine; Fletcher, Olivia; Flyger, Henrik; Fritschi, Lin; Gabrielson, Marike; Gago-Dominguez, Manuela; García-Closas, Montserrat; Giles, Graham G; González-Neira, Anna; Guénel, Pascal; Hahnen, Eric; Haiman, Christopher A; Hall, Per; Hollestelle, Antoinette; Hoppe, Reiner; Hopper, John L; Howell, Anthony; Jager, Agnes; Jakubowska, Anna; John, Esther M; Johnson, Nichola; Jones, Michael E; Jung, Audrey; Kaaks, Rudolf; Keeman, Renske; Khusnutdinova, Elza; Kitahara, Cari M; Ko, Yon-Dschun; Kosma, Veli-Matti; Koutros, Stella; Kraft, Peter; Kristensen, Vessela N; Kubelka-Sabit, Katerina; Kurian, Allison W; Lacey, James V; Lambrechts, Diether; Larson, Nicole L; Linet, Martha; Ogrodniczak, Alicja; Mannermaa, Arto; Manoukian, Siranoush; Margolin, Sara; Mavroudis, Dimitrios; Milne, Roger L; Muranen, Taru A; Murphy, Rachel A; Nevanlinna, Heli; Olson, Janet E; Olsson, Håkan; Park-Simon, Tjoung-Won; Perou, Charles M; Peterlongo, Paolo; Plaseska-Karanfilska, Dijana; Pylkäs, Katri; Rennert, Gad; Saloustros, Emmanouil; Sandler, Dale P; Sawyer, Elinor J; Schmidt, Marjanka K; Schmutzler, Rita K; Shibli, Rana; Smeets, Ann; Soucy, Penny
Source
Communications Biology. 5(1)
Subject
Language
Abstract
Germline copy number variants (CNVs) are pervasive in the human genome but potential disease associations with rare CNVs have not been comprehensively assessed in large datasets. We analysed rare CNVs in genes and non-coding regions for 86,788 breast cancer cases and 76,122 controls of European ancestry with genome-wide array data. Gene burden tests detected the strongest association for deletions in BRCA1 (P = 3.7E-18). Nine other genes were associated with a p-value