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Fig. 1 | Genome Medicine

Fig. 1

From: Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases

Fig. 1

Summary of PCNV/UPD findings from the quality control array and CMA. a A pie chart to show the types of aberrations detected by the QC array. b A table to show the proportion of patients with PCNVs/UPD from the QC array that were known or unknown prior to ES testing. c A pie chart to show the types of aberrations detected by CMA. d A chart to correlate the findings from the QC array and those from CMA. “+” means with PCNV/UPD from the QC array or CMA; “-” means without PCNV/UPD findings

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Genome Medicine

ISSN: 1756-994X

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