Fig. 1
From: Prenatal diagnosis of rearrangements in the fetal 22q11.2 region
Karyotype analysis, BoBs™ analysis, SNP-array analysis, and FISH analysis. a Karyotype of P3, normal karyotype. b BoBs™ analysis of P5. The arrow indicates DiGeorge syndrome region amplification. c SNP-array analysis of P5. The thick blue line indicates duplication of the 22q11.2 region. d SNP-array analysis of P3. The thick red line indicates deletion of the 22q11.2 region. e FISH analysis of P5. N25 (red) indicates duplication of the DiGeorge region