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Submicroscopic aberrations of chromosome 16 in prenatal diagnosis

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Figure

Fig. 1 The frequency of 134 submicroscopic anomalies on each chromosome. All chromosomes except for chromosome 12 were involved.Among them, 11.1% (15/134) aberration derived from chromosome 16, which had the highest frequency, followed by chromosome 2, 22 and X
Table 1 Characterization of the 15 submicroscopic aberrations associated with chromosome 16 detected from 14 patients
Fig. 2 SNP array results for the individual of UPD(16). SNP array analysis revealed two copies of neutral LOH of 19.2 Mb in 16p13.3p12.3(red arrow) and 10.3 Mb in 16q23.2q24.3 (black arrow) regions, respectively

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