Rare germline copy number variants (CNVs) and breast cancer risk.
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ICR Authors
Authors
Dennis, J
Tyrer, JP
Walker, LC
Michailidou, K
Dorling, L
Bolla, MK
Wang, Q
Ahearn, TU
Andrulis, IL
Anton-Culver, H
Antonenkova, NN
Arndt, V
Aronson, KJ
Freeman, LEB
Beckmann, MW
Behrens, S
Benitez, J
Bermisheva, M
Bogdanova, NV
Bojesen, SE
Brenner, H
Castelao, JE
Chang-Claude, J
Chenevix-Trench, G
Clarke, CL
NBCS Collaborators,
Collée, JM
CTS Consortium,
Couch, FJ
Cox, A
Cross, SS
Czene, K
Devilee, P
Dörk, T
Dossus, L
Eliassen, AH
Eriksson, M
Evans, DG
Fasching, PA
Figueroa, J
Fletcher, O
Flyger, H
Fritschi, L
Gabrielson, M
Gago-Dominguez, M
García-Closas, M
Giles, GG
González-Neira, A
Guénel, P
Hahnen, E
Haiman, CA
Hall, P
Hollestelle, A
Hoppe, R
Hopper, JL
Howell, A
ABCTB Investigators,
kConFab/AOCS Investigators,
Jager, A
Jakubowska, A
John, EM
Johnson, N
Jones, ME
Jung, A
Kaaks, R
Keeman, R
Khusnutdinova, E
Kitahara, CM
Ko, Y-D
Kosma, V-M
Koutros, S
Kraft, P
Kristensen, VN
Kubelka-Sabit, K
Kurian, AW
Lacey, JV
Lambrechts, D
Larson, NL
Linet, M
Ogrodniczak, A
Mannermaa, A
Manoukian, S
Margolin, S
Mavroudis, D
Milne, RL
Muranen, TA
Murphy, RA
Nevanlinna, H
Olson, JE
Olsson, H
Park-Simon, T-W
Perou, CM
Peterlongo, P
Plaseska-Karanfilska, D
Pylkäs, K
Rennert, G
Saloustros, E
Sandler, DP
Sawyer, EJ
Schmidt, MK
Schmutzler, RK
Shibli, R
Smeets, A
Soucy, P
Southey, MC
Swerdlow, AJ
Tamimi, RM
Taylor, JA
Teras, LR
Terry, MB
Tomlinson, I
Troester, MA
Truong, T
Vachon, CM
Wendt, C
Winqvist, R
Wolk, A
Yang, XR
Zheng, W
Ziogas, A
Simard, J
Dunning, AM
Pharoah, PDP
Easton, DF
Tyrer, JP
Walker, LC
Michailidou, K
Dorling, L
Bolla, MK
Wang, Q
Ahearn, TU
Andrulis, IL
Anton-Culver, H
Antonenkova, NN
Arndt, V
Aronson, KJ
Freeman, LEB
Beckmann, MW
Behrens, S
Benitez, J
Bermisheva, M
Bogdanova, NV
Bojesen, SE
Brenner, H
Castelao, JE
Chang-Claude, J
Chenevix-Trench, G
Clarke, CL
NBCS Collaborators,
Collée, JM
CTS Consortium,
Couch, FJ
Cox, A
Cross, SS
Czene, K
Devilee, P
Dörk, T
Dossus, L
Eliassen, AH
Eriksson, M
Evans, DG
Fasching, PA
Figueroa, J
Fletcher, O
Flyger, H
Fritschi, L
Gabrielson, M
Gago-Dominguez, M
García-Closas, M
Giles, GG
González-Neira, A
Guénel, P
Hahnen, E
Haiman, CA
Hall, P
Hollestelle, A
Hoppe, R
Hopper, JL
Howell, A
ABCTB Investigators,
kConFab/AOCS Investigators,
Jager, A
Jakubowska, A
John, EM
Johnson, N
Jones, ME
Jung, A
Kaaks, R
Keeman, R
Khusnutdinova, E
Kitahara, CM
Ko, Y-D
Kosma, V-M
Koutros, S
Kraft, P
Kristensen, VN
Kubelka-Sabit, K
Kurian, AW
Lacey, JV
Lambrechts, D
Larson, NL
Linet, M
Ogrodniczak, A
Mannermaa, A
Manoukian, S
Margolin, S
Mavroudis, D
Milne, RL
Muranen, TA
Murphy, RA
Nevanlinna, H
Olson, JE
Olsson, H
Park-Simon, T-W
Perou, CM
Peterlongo, P
Plaseska-Karanfilska, D
Pylkäs, K
Rennert, G
Saloustros, E
Sandler, DP
Sawyer, EJ
Schmidt, MK
Schmutzler, RK
Shibli, R
Smeets, A
Soucy, P
Southey, MC
Swerdlow, AJ
Tamimi, RM
Taylor, JA
Teras, LR
Terry, MB
Tomlinson, I
Troester, MA
Truong, T
Vachon, CM
Wendt, C
Winqvist, R
Wolk, A
Yang, XR
Zheng, W
Ziogas, A
Simard, J
Dunning, AM
Pharoah, PDP
Easton, DF
Document Type
Journal Article
Date
2022-01-18
Date Accepted
2021-12-01
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 < 0.01 including known susceptibility genes CHEK2 (P = 0.0008), ATM (P = 0.002) and BRCA2 (P = 0.008). Outside the known genes we detected associations with p-values < 0.001 for either overall or subtype-specific breast cancer at nine deletion regions and four duplication regions. Three of the deletion regions were in established common susceptibility loci. To the best of our knowledge, this is the first genome-wide analysis of rare CNVs in a large breast cancer case-control dataset. We detected associations with exonic deletions in established breast cancer susceptibility genes. We also detected suggestive associations with non-coding CNVs in known and novel loci with large effects sizes. Larger sample sizes will be required to reach robust levels of statistical significance.
Citation
Communications biology, 2022, 5 (1), pp. 65 - ?
Source Title
Publisher
NATURE PORTFOLIO
ISSN
2399-3642
eISSN
2399-3642
2399-3642
2399-3642
Research Team
Functional Genetic Epidemiology
Aetiological Epidemiology
Aetiological Epidemiology