Fig. 2From: A novel frame-shift deletion in FANCF gene causing autosomal recessive Fanconi anemia: a case reporta: Pedigree, b: NGS data on IGV, and c: Sanger sequencing chromatogram. In the pedigree, proband is shown as a product of consanguineous marriage and the first case affected by FA in this family. Bam file data of the patient show the homozygous deletion (left). Sanger sequencing and NCBI blast confirmed this homozygous deletion (right)Back to article page