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  • Structural Aberrations with Secondary Implications (SASIs): consensus recommendations for reporting of cancer susceptibility genes identified during analysis of Copy Number Variants (CNVs)

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Cancer genetics
Position statement
Structural Aberrations with Secondary Implications (SASIs): consensus recommendations for reporting of cancer susceptibility genes identified during analysis of Copy Number Variants (CNVs)

Authors

  1. Correspondence to Dr Clare Turnbull, Division of Genetics and Epidemiology, Institute of Cancer Research, Sutton SM2 5RG, UK; clare.turnbull{at}icr.ac.uk
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Citation

Talukdar S, Hawkes L, Hanson H on behalf of UK Association for Clinical Genomic Science and UK Cancer Genetics Group, et al
Structural Aberrations with Secondary Implications (SASIs): consensus recommendations for reporting of cancer susceptibility genes identified during analysis of Copy Number Variants (CNVs)
Journal of Medical Genetics 2019;56:718-726.

Publication history

  • Received October 25, 2018
  • Revised February 19, 2019
  • Accepted March 2, 2019
  • First published April 24, 2019.
Online issue publication 
October 23, 2019

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© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.