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Additional file 2: Fig. S1. Additional evidence for causative role of the de novo deletion 3p22.1. A���NGS results using IGV software showing homozygosity for all genetic variations found at locus. RPSA in patient with asplenia. B, C���SNP array results of the mother and father, respectively, showing no copy number variations at 3p22.1.

Additional file 1: Table S1. The panel used in the study, including genes whose defects lead to primary immunodeficiencies and hematological disorders.