Background: 22q11.2 deletion syndrome (22q11.2DS) is a disorder caused when a small part of chromosome 22 is missing. Diagnosis is currently established by the identification of a heterozygous deletio
Summary of targeted sequencing data in multiple replicates for dCATCH-Seq and CATCH-Seq. Table S2. Comparison of Indel calls between dCATCH-Seq and CATCH-Seq. Table S3. HLA gene typing for dCATCH-Seq.
