This dataset includes bam files from 58 samples. These bam files include all read pairs where at least one of the reads aligns within 1kb of the HTT repeat expansion. These samples were sequenced usin
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
Although we targeted putative promoter regions of all of the genes (i.e., 4 kb upstream of the transcription start site where annotated), we also targeted complete exonic regions (indicated by *) or g
Targeted regions of the genome were sequenced as part of the ENCODE project's comparative genomics analysis. Additional targets were selected for the Comparative Vertebrate Sequencing project.