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. 2022 Jan 24;13:780930. doi: 10.3389/fgene.2022.780930

FIGURE 3.

FIGURE 3

Characterization of the identified 18p deletion analyzed by WGS. (A) WGS data showing the proband carries a heterozygous deletion at chromosome 18p11.32-11.21 (chr18:10,001-15,199,661) x1 (h19). (B) A view of deleted disease-associated genes in the patient in the DECIPHER database.