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

Global variation of copy number in the MCF7 genome

SNP array analysis of neuroblastic tumor NB99

Affymetrix SNP and CNV data for the HuRef individual

Illumina SNP and CNV data for the HuRef individual

Intellectual disability and mood disorder associated with partial deletion of the Neurexin 1 Gene

ENPP1 deletion and infantile arterial calcification

Copy number profiling of PEO1 ovarian cancer cell line

COLO320 DNA copy number analysis

SNP array for CNV calling AUTS2 project [Illumina]

CNV and LOH analysis of patient sample PN11-0204

SNP array data for embryonal rhabdomyosarcoma in a patient with Costello syndrome

Single case sample of a Non-Hodgkin lymphoma

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

Affymetrix CytoScan HD array data for patient with Intellectual Disabilities

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

Application of SNP-array for the detection of genomic rearrangements responsible for sindromic mental retardation of unknown cause

Affymetrix CytoScan 750K array data for a parthenogenetic SMA human embryonic stem cell line

Loss-of-function mutations TDRD7 lead to a rare novel syndrome combining congenital cataract and non-obstructive azoospermia in humans

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