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16p13.11 microdeletion syndrome detected by chromosomal microarray (CMA) and Next‐Generation Sequencing (NGS) on single‐cell circulating extravillous trophoblasts (cEVTs) analysis. Profile of the 800Kb deletion within the 16p13.11 region (chr16:15500000–16300000) in 2 out of 2 cEVTs recovered from the same pregnancy (case M087). Highlighted in light green is the largest 16p13.11 region involved in the syndrome (3.3 Mb); while in dark green is depicted its critical region.
