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. 2018 Nov 19;38(13):1069–1078. doi: 10.1002/pd.5377

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© 2018 The Authors Prenatal Diagnosis Published by John Wiley & Sons Ltd

This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

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Detection of a 6.0‐Mb deletion of 1p35.1p34.3 in a male fetal cell. The whole genome plot for the cell‐based noninvasive prenatal testing (NIPT) result is shown in Panel A, demonstrating the comparison to a female fetal reference cell with the X and Y chromosome difference and showing a deletion on chromosome 1. The single chromosome 1 plot is shown in Panel B. The data are concordant with the chorionic villus sampling (CVS) chromosomal microarray (CMA) data shown in Panel C. The coordinates for the deletion from the array were chr1:33,058,933‐39,031,717 [Colour figure can be viewed at wileyonlinelibrary.com]