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. 2009 Sep;19(9):1682–1690. doi: 10.1101/gr.083501.108

Table 3.

Assessment of CNVs detected in a patient with multiple congenital anomalies

graphic file with name 1682tbl3.jpg

(OR gene) Olfactory receptor gene; (SD region) region of known segmental duplication (RefSeq gene transcript overlap was used for gene assessment); (P.T.) parental transmission. Boldface indicates the putative pathogenic CNV.