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Related Experiment Video

Updated: Sep 26, 2025

Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants

Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants

Published on: February 21, 2015

Editorial: Copy Number Variation in Rare Disorders

Katalin Komlósi¹, Attila Gyenesei², Judit Bene³

¹Institute of Human Genetics, Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Frontiers in Genetics

|April 22, 2022

Summary

No abstract available in PubMed .

Keywords:

Mendelian disease copy number variation (CNV)genomic disorders genomic rearrangement rare disorders

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