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Figure 5 | BMC Genomics

Figure 5

From: A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease

Figure 5

Chromosome 8 CNVs detected by chromosomal microarray, CNVplex® and MLPA. A. Microarray profile of chromosome 8 showing a deletion at 8pter–8p23.1 and a duplication at 8p23.1–8p22. B. CNVplex® probes set in 8p and results inferred from the signal. Green boxes are probes, and solid-colored bars below the map depict the results. C. Data of MLPA analysis. The dots represent MLPA probes, and the lines indicate the threshold.

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