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. 2022 Aug 26;12:14589. doi: 10.1038/s41598-022-14161-6

Figure 1.

Figure 1

Patient characteristics and information on detected variants. Each column indicates one patient. SNV single-nucleotide variant, CNV copy number variant, UPD uniparental disomy, AD autosomal dominant, AR autosomal recessive, XLD X-linked dominant, XLR X-linked recessive.