ArrayCGH on a cohort of pediatric T-ALL cases characterized by TCRAD-MYC translocation. ArrayCGH on a cohort of pediatric T-ALL cases characterized by TCRAD-MYC translocation

ArrayCGH was performed on a cohort of 25 specimens collected from children with newly diagnosed T-ALL characterized by TCRAD-MYC translocation ArrayCGH analyses were perfomed to study genomic aberrations occurring in the rare subgroup of TCRAD-MYC rearranged T-ALL Overall design: 25 DNA samples from pediatric T-ALL patients at diagnosis were analyzed on the Agilent SurePrint G3 Human CGH microarrays (G4449A, design ID: 022060). For every sample, the gender-matched control was labeled in parallel and hybridized together