[Application of bionano optical mapping for the diagnosis of a 16p11.2-p12.2 microdeletion]

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Oct 10;37(10):1167-1171. doi: 10.3760/cma.j.cn511374-20190906-00458.
[Article in Chinese]

Abstract

Objective: To delineate chromosomal aberration caused by structural chromosomal abnormalities with bionano optical mapping.

Methods: Chromosomal karyotyping, bionano optical mapping and copy number variation sequencing (CNV-seq) were used to delineate the chromosomal aberration carried by a patient.

Results: The patient was found to have an anomalous chromosome 16 by karyotyping analysis, which was verified by bionano optical mapping and CNV-seq as loss of heterozygosity at 16p11.2-p12.2.

Conclusion: Bionano optical mapping has provided a novel tool for the detection and diagnosis of structural chromosomal aberrations.

MeSH terms

  • Chromosome Deletion*
  • Chromosome Disorders* / diagnosis
  • Chromosome Disorders* / genetics
  • Chromosomes, Human, Pair 16
  • DNA Copy Number Variations*
  • Humans
  • Karyotyping