Additional file 6 of Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants

Additional file 6 SVs identified in Family 2. All rare SVs (AF < 0.003 in SweGen) shared by the affected individuals in Family 2.

附加文件6：家族2中鉴定得到的结构变异（Structural Variants, SVs）。所有在家族2受累个体中共同携带的罕见结构变异，其等位基因频率（Allele Frequency, AF）在SweGen数据库中小于0.003。