10 Intellectual Disability samples for clinically relevant CNV detection

11p11.12p12 duplication in a family with intellectual disability and craniofacial anomalies

14q32 recombinations deregulating BCL11B mark a distinct Mixed Phenotype Leukemia

7q11.23 dosage-dependent dysregulation in the human pluripotent state primes aberrant transcriptional programs in disease-relevant lineages

7q11.23 dosage-dependent dysregulation in the human pluripotent state primes aberrant transcriptional programs in disease-relevant lineages (aCGH)

A Genomic Portrait of Resectable Hepatocellular Carcinomas: Implications of RB1 and FGF19 Aberrations for Patient Stratification.

A High-Resolution Copy Number Variation Resource for Clinical Genetics

A Novel Silent Mutation in the L1CAM Gene causing Fetal Hydrocephalus

A novel t(X;21) (p11.4;q22.12) translocation adds to the role of BCOR and RUNX1 in Myelodysplastic Syndromes/Acute Myeloid Leukemias

A novel t(X;21) (p11.4;q22.12) translocation adds to the role of BCOR and RUNX1 in Myelodysplastic Syndromes/Acute Myeloid Leukemias [Copy number analysis]

A prenatal diagnosis case of partial duplication 21q21.1-q21.2 with normal phenotype maternally inherited

Affymetric SNP Array Data of 45 liver metastasis samples from colorectal cancer patients

Affymetrix CytoScan array data for leukemia cell lines

Affymetrix CytoScan array data for leukemia cell lines TK6 and WIL2-NS

Affymetrix CytoScan 750K and HD data for developmental delay and/or physical disability phenotypes samples

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

Affymetrix CytoScan 750K data for validation of the BoBs/CNV-seq comparison study

Affymetrix CytoScan HD and OncoScan array data for malignant melanoma samples

Affymetrix CytoScan HD array data for patient with Intellectual Disabilities

Affymetrix CytoScan HD array data of iPSCs and iPSC-derived-NSPCs