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. 2021 Jul 20;14:38. doi: 10.1186/s13039-021-00555-0

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© The Author(s) 2021

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 6 — Possible inversion recombinant correction in case 3. A NIPT study, referred due to a cardiac lesion, showing a terminal deletion of 1p and a duplication of terminal 1q (A), with both equivalent to the 13% fetal fraction, consistent with non-mosaic fetal alterations. B Subsequent microarray analysis at 23 weeks of gestation showed no dosage changes of chromosome 1, although a 21.58 Mb terminal 1p ROH was present (B)