Correction: 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)

Affiliations

¹ Autism & Developmental Medicine Institute, Geisinger, Danville, PA, USA. documents@acmg.net.
² ARUP Laboratories, Salt Lake City, UT, USA.
³ Department of Pathology, University of Utah, Salt Lake City, UT, USA.
⁴ Stanford University School of Medicine, Stanford, CA, USA.
⁵ Quest Diagnostics Nichols Institute, San Juan Capistrano, CA, USA.
⁶ Genomics Laboratory, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
⁷ Lineagen, Salt Lake City, UT, USA.
⁸ Children's Hospital Los Angeles, Los Angeles, CA, USA.
⁹ Texas Children's Cancer Center, Baylor College of Medicine, Houston, TX, USA.
¹⁰ AncestryDNA, Lehi, UT, USA.
¹¹ Invitae, San Francisco, CA, USA.
¹² Autism & Developmental Medicine Institute, Geisinger, Danville, PA, USA.

Free article

Published Erratum

Erin Rooney Riggs et al. Genet Med. 2021 Nov.

Free article

. 2021 Nov;23(11):2230.

doi: 10.1038/s41436-021-01150-9.

¹ Autism & Developmental Medicine Institute, Geisinger, Danville, PA, USA. documents@acmg.net.
² ARUP Laboratories, Salt Lake City, UT, USA.
³ Department of Pathology, University of Utah, Salt Lake City, UT, USA.
⁴ Stanford University School of Medicine, Stanford, CA, USA.
⁵ Quest Diagnostics Nichols Institute, San Juan Capistrano, CA, USA.
⁶ Genomics Laboratory, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
⁷ Lineagen, Salt Lake City, UT, USA.
⁸ Children's Hospital Los Angeles, Los Angeles, CA, USA.
⁹ Texas Children's Cancer Center, Baylor College of Medicine, Houston, TX, USA.
¹⁰ AncestryDNA, Lehi, UT, USA.
¹¹ Invitae, San Francisco, CA, USA.
¹² Autism & Developmental Medicine Institute, Geisinger, Danville, PA, USA.

No abstract available

Erratum for

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).
Riggs ER, Andersen EF, Cherry AM, Kantarci S, Kearney H, Patel A, Raca G, Ritter DI, South ST, Thorland EC, Pineda-Alvarez D, Aradhya S, Martin CL. Riggs ER, et al. Genet Med. 2020 Feb;22(2):245-257. doi: 10.1038/s41436-019-0686-8. Epub 2019 Nov 6. Genet Med. 2020. PMID: 31690835 Free PMC article.