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

Illumina SNP and CNV data for the HuRef individual

ENPP1 deletion and infantile arterial calcification

Copy number profiling of PEO1 ovarian cancer cell line

SNP array for CNV calling AUTS2 project [Illumina]

Generation and Characterization of an immortalized human mesenchymal stromal cell line model [Affymetrix]

De novo homozygous deletion of segmental KAL1 and entire STS cause Kallmann syndrome and X-linked ichthyosis in a Chinese family

aCGH of chromosome X in a female patient with ALL and Leri-Weill syndrome

Tetra-Amelia with lung aplasia phenotype

Detection of CNVs in patients with syndromic intellectual disability

Hypodiploidy in a pediatric patient of T-cell acute lymphoblastic leukemia: a case report

AGAP3: a novel BRAF-fusion partner in pediatric pancreatic acinar cell carcinoma

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

Human SUP-B15 cells: CNV compared to reference genome.

U87MG Decoded: The Genomic Sequence of a Cytogenetically Aberrant Human Cancer Cell Line

Evaluation of copy number alterations in the Ewing's Sarcoma cell line SKES1 with Affymetrix 500k SNP microarray

Genotyping data from one patient with unexplained mental retardation and a deletion in 15q13

Homozygosity mapping in a consanguineous family with osteogenesis imperfecta (OI)

Emergence of Non-Random Chromosomal Alterations (Trisomy 7 and 20) Derived from Diploid Human Colonic Epithelial Cells

LIF-Dependent, Pluripotent Stem Cells Established from Inner Cell Mass of Porcine Embryos