Please cite the X-CNV method and the ACMG/ClinGen CNV standard when
using the corresponding package lanes:

  Zhang L, Shi J, Ouyang J, Zhang R, Tao Y, Yuan D, Lv C, Wang R, Ning
  B, Roberts R, Tong W, Liu Z, Shi T (2021). “X-CNV: genome-wide
  prediction of the pathogenicity of copy number variations.” _Genome
  Medicine_, *13*(1), 132. doi:10.1186/s13073-021-00945-4
  <https://doi.org/10.1186/s13073-021-00945-4>.

A BibTeX entry for LaTeX users is

  @Article{,
    title = {X-CNV: genome-wide prediction of the pathogenicity of copy number variations},
    author = {Lu Zhang and Jing Shi and Jing Ouyang and Rui Zhang and Yan Tao and Dong Yuan and Cong Lv and Rui Wang and Bing Ning and Richard Roberts and William Tong and Zhi Liu and Tao Shi},
    journal = {Genome Medicine},
    year = {2021},
    volume = {13},
    number = {1},
    pages = {132},
    doi = {10.1186/s13073-021-00945-4},
    pmid = {34407882},
  }

  Riggs E, Andersen E, Cherry A, Martin C (2020). “Technical standards
  for the interpretation and reporting of constitutional copy-number
  variants: a joint consensus recommendation of the American College of
  Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource
  (ClinGen).” _Genetics in Medicine_, *22*, 245-257.
  doi:10.1038/s41436-019-0686-8
  <https://doi.org/10.1038/s41436-019-0686-8>.

A BibTeX entry for LaTeX users is

  @Article{,
    title = {Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen)},
    author = {Erin Rooney Riggs and Erica F Andersen and Athena M Cherry and Christa Lese Martin},
    journal = {Genetics in Medicine},
    year = {2020},
    volume = {22},
    pages = {245--257},
    doi = {10.1038/s41436-019-0686-8},
    pmid = {31690835},
  }