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. 2019 Nov 20;10:1162. doi: 10.3389/fgene.2019.01162

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Copyright © 2019 Chai, DiAdamo, Grommisch, Xu, Zhou, Wen, Mahoney, Bale, McGrath, Spencer-Manzon, Li and Zhang

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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The ADR and RF of cytogenomic abnormalities detected in prenatal and pediatric settings. (A) The composite ADR of cytogenomic abnormalities in prenatal and pediatric settings. (B/C) The RF for the spectrum of chromosomal abnormalities and the spectrum of pCNVs in prenatal and pediatric settings. The red dot line separates the abnormalities into two groups per classification. ADR, abnormality detection rate; b-Rob, balanced Robertsonian translocations; chr abn, chromosomal abnormality; del/dup, deletion/duplication; inter-pCNV, interstitial pCNV; OA, other aneuploidy; OBR, other balanced rearrangements; pCNVs, pathogenic copy number variants; RF, relative frequency; subtel-pCNV, subtelomeric pCNV; T21, trisomy 21; T18, trisomy 18; T13, trisomy 13; Tri/tetra, triploid and tetraploid; UR, unbalanced rearrangements.