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. 2020 Oct 22;11:568052. doi: 10.3389/fgene.2020.568052

TABLE 2.

CNVs recurrent in at least two families.

Genes Recurrent subjects Related disease
UGT2B17 TWS01| TWS06| TWS18| TWS12 Osteoporosis
OVOS XH1535| TWS06| TWS18| TWS22 Unknown
KATNAL2 TWS06| TWS12 Autism