Additional file 2 of Using synthetic chromosome controls to evaluate the sequencing of difficult regions within the human genome

Additional file 2. ChrQ cytoband: file containing the coordinates for the different regions of chrQ (p1) small variants (including SNPs and indels) and simple repeats, (p2) structural variants (including large insertions, deletions, duplications, inversions and translocations), (p3) HLA genes and (p4) immune receptor genes.

附加文件2：Q染色体细胞带（ChrQ cytoband）文件，包含Q染色体各区域的坐标信息：(p1) 小变异（涵盖单核苷酸多态性（Single Nucleotide Polymorphisms, SNPs）、插入缺失变异（Insertions-Deletions, indels）与简单重复序列）；(p2) 结构变异（涵盖大片段插入、缺失、重复、倒位及易位）；(p3) 人类白细胞抗原（HLA）基因；(p4) 免疫受体基因。