Fig. 2From: A sporadic case of congenital aniridia caused by pericentric inversion inv(11)(p13q14) associated with a 977 kb deletion in the 11p13 regiona. Patient’s karyotype. b. Detailed view on derivative chromosome 11 and ideogram view. c. FISH analysis on WT1 locus. d. MLPA analysis for the 11p13 region. e. CMA analysis of the 11p13 regionBack to article page