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Updated: Aug 14, 2026

Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants
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Case Report: Neuroblastoma Breakpoint Family Genes Associate With 1q21 Copy Number Variation Disorders

Lijuan Zhu1, Xiaoji Su1

  • 1Children's Hospital of Fudan University Anhui Hospital, Hefei, China.

Frontiers in Genetics
|October 14, 2021
PubMed

Keywords:
1q21.2Olduvai domaincongenital heart diseasehearing lossmicroduplication

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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
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