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Fig. 1 | Molecular Cytogenetics

Fig. 1

From: Noninvasive prenatal testing for the detection of fetal chromosome 17 microduplication: clinical implications and findings

Fig. 1

Overview of Case 1 from by NIPT, Karyotype analysis and CMA. A A NIPT study of maternal plasma showing a Z-score of 8.97 for fetal chromosome 17 and a duplication of 2 Mb from 34.5 to 36.5 Mb region. B Karyotype analysis of maternal amniotic fluid showing no significant fetal chromosomal abnormalities. C CMA analysis of amniotic fluid showing that a duplication of 1.9 Mb on chromosome 17q12 (arr [GRCh37] 17q12 (34,440,088–36,311,009) × 3). D CMA analysis of maternal peripheral blood showing that a duplication of 1.9 Mb on chromosome 17q12 (arr [GRCh37] 17q12 (34,405,514–36,307,773) × 3)

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Molecular Cytogenetics

ISSN: 1755-8166