Phenotypic manifestations of copy number variation in chromosome 16p13.11

Sandesh C Sreenath Nagamani, Ayelet Erez, Patricia Bader, Seema R. Lalani, Daryl A. Scott, Fernando Scaglia, Sharon E. Plon, Anne Tsai, Tyler Reimschisel, Elizabeth Roeder, Amy D. Malphrus, Patricia A. Eng, Patricia M. Hixson, Sung Hae L Kang, Pawel Stankiewicz, Ankita Patel, Sau Wai Cheung

Research output: Contribution to journalArticle

57 Citations (Scopus)

Abstract

The widespread clinical utilization of array comparative genome hybridization, has led to the unraveling of many new copy number variations (CNVs). Although some of these CNVs are clearly pathogenic, the phenotypic consequences of others, such as those in 16p13.11 remain unclear. Whereas deletions of 16p13.11 have been associated with multiple congenital anomalies, the relevance of duplications of the region is still being debated. We report detailed clinical and molecular characterization of 10 patients with duplication and 4 patients with deletion of 16p13.11. We found that patients with duplication of the region have varied clinical features including behavioral abnormalities, cognitive impairment, congenital heart defects and skeletal manifestations, such as hypermobility, craniosynostosis and polydactyly. These features were incompletely penetrant. Patients with deletion of the region presented with microcephaly, developmental delay and behavioral abnormalities as previously described. The CNVs were of varying sizes and were likely mediated by non-allelic homologous recombination between low copy repeats. Our findings expand the repertoire of clinical features observed in patients with CNV in 16p13.11 and strengthen the hypothesis that this is a dosage sensitive region with clinical relevance.

Original languageEnglish (US)
Pages (from-to)280-286
Number of pages7
JournalEuropean Journal of Human Genetics
Volume19
Issue number3
DOIs
StatePublished - Mar 2011
Externally publishedYes

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Chromosomes
Genomic Segmental Duplications
Polydactyly
Craniosynostoses
Microcephaly
Comparative Genomic Hybridization
Congenital Heart Defects
Homologous Recombination

Keywords

  • 16p13.11
  • behavioral abnormality
  • CNV
  • cognitive impairment

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

Nagamani, S. C. S., Erez, A., Bader, P., Lalani, S. R., Scott, D. A., Scaglia, F., ... Cheung, S. W. (2011). Phenotypic manifestations of copy number variation in chromosome 16p13.11. European Journal of Human Genetics, 19(3), 280-286. https://doi.org/10.1038/ejhg.2010.184

Phenotypic manifestations of copy number variation in chromosome 16p13.11. / Nagamani, Sandesh C Sreenath; Erez, Ayelet; Bader, Patricia; Lalani, Seema R.; Scott, Daryl A.; Scaglia, Fernando; Plon, Sharon E.; Tsai, Anne; Reimschisel, Tyler; Roeder, Elizabeth; Malphrus, Amy D.; Eng, Patricia A.; Hixson, Patricia M.; Kang, Sung Hae L; Stankiewicz, Pawel; Patel, Ankita; Cheung, Sau Wai.

In: European Journal of Human Genetics, Vol. 19, No. 3, 03.2011, p. 280-286.

Research output: Contribution to journalArticle

Nagamani, SCS, Erez, A, Bader, P, Lalani, SR, Scott, DA, Scaglia, F, Plon, SE, Tsai, A, Reimschisel, T, Roeder, E, Malphrus, AD, Eng, PA, Hixson, PM, Kang, SHL, Stankiewicz, P, Patel, A & Cheung, SW 2011, 'Phenotypic manifestations of copy number variation in chromosome 16p13.11', European Journal of Human Genetics, vol. 19, no. 3, pp. 280-286. https://doi.org/10.1038/ejhg.2010.184
Nagamani SCS, Erez A, Bader P, Lalani SR, Scott DA, Scaglia F et al. Phenotypic manifestations of copy number variation in chromosome 16p13.11. European Journal of Human Genetics. 2011 Mar;19(3):280-286. https://doi.org/10.1038/ejhg.2010.184
Nagamani, Sandesh C Sreenath ; Erez, Ayelet ; Bader, Patricia ; Lalani, Seema R. ; Scott, Daryl A. ; Scaglia, Fernando ; Plon, Sharon E. ; Tsai, Anne ; Reimschisel, Tyler ; Roeder, Elizabeth ; Malphrus, Amy D. ; Eng, Patricia A. ; Hixson, Patricia M. ; Kang, Sung Hae L ; Stankiewicz, Pawel ; Patel, Ankita ; Cheung, Sau Wai. / Phenotypic manifestations of copy number variation in chromosome 16p13.11. In: European Journal of Human Genetics. 2011 ; Vol. 19, No. 3. pp. 280-286.
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