DNA copy number variation from human Wilms' Tumor samples

Metastatic potential is determined early in synovial sarcoma development and reflected by tumor molecular features [aCGH]

Pan-genomic study of primary human retinoblastoma samples

Copy number profiling of 556 high-risk neuroblastoma patients using aCGH or SNP arrays

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

Determination of CNVs in SKOV3 cells knocked down in BECN1 or MAP1LC3B

Large B-Cell Lymphomas in Pediatric and Young Adults Display Clinically Relevant Molecular Features Distinguishable from Adult Counterparts

CytoScan HD array data from Human mammary epithelian cells after Cyclin E overexpression

Copy-Number abberation profiles of glioma patient tissue samples and corresponding xenografted tumor samples as well as cell lines derived there-of

Human HFF cells large rearranements detection after CRISPR-Cas9 nuclease (Fig.2c)

Human HFF cells large rearrangements detection after CRISPR-Cas9 nuclease (Fig. 3d)

Human HFF cells large rearrangements detection after CRISPR-Cas9 nuclease (Supplentary Fig. 4)

DNA copy numbers of malignant glioma in culture

aCGH data from age-dichotomized ER+ breast tumors

Ovarian cancer cell line study

PI3K inhibition in ER+ breast cancer microarray data

Multiple chromosomal monosomies are characteristic of giant cell ependymoma

Natural genetic variation caused by small insertions and deletions in the human genome

Genome-wide array comparative genomic hybridization (aCGH) profiling of endothelial progenitor cells, and their comparison to tumor plasma cells, in multiple myeloma

Landscape of somatic allelic imbalances and copy number alterations in human lung carcinoma