Simultaneous analysis of the NGS H‐TAD gene panel and SNP array revealed that the heterozygous deletion of SCARF2 was part of a 22q11.2 deletion (i.e., DiGeorge syndrome) (3.2Mb; hg19; chr22:20779645_20792061). This evidence concerns the gene SCARF2 and 22q11.2 deletion syndrome.