1539 series
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Accession Title Series type(s) Organism(s) Samples GDS Supplementary Contact Release date
Remove filtersFilter Remove filterGenome variation profiling by SNP array
GSE103123
Copy number profiling of 556 high-risk neuroblastoma patients using aCGH or SNP arrays
Katleen De Preter Mar 13, 2018
GSE8508
Global variation of copy number in the MCF7 genome
1 Toshio Kojima Feb 08, 2008
GSE12461
SNP array analysis of neuroblastic tumor NB99
  • Genome variation profiling by SNP array
1 Olivier Delattre Oct 16, 2008
GSE20275
Affymetrix SNP and CNV data for the HuRef individual
1 Andy Pang Feb 12, 2013
GSE20284
Illumina SNP and CNV data for the HuRef individual
1 Andy Pang Feb 12, 2013
GSE23358
Intellectual disability and mood disorder associated with partial deletion of the Neurexin 1 Gene
  • Genome variation profiling by SNP array
1 Patricia Bray-Ward Jun 25, 2011
GSE26860
ENPP1 deletion and infantile arterial calcification
1 Scott Watkins Jan 26, 2011
GSE29256
Copy number profiling of PEO1 ovarian cancer cell line
  • Genome variation profiling by SNP array
1 Charlotte K Y Ng Jun 30, 2011
GSE30182
COLO320 DNA copy number analysis
  • Genome variation profiling by SNP array
1 Keyan Salari Nov 02, 2012
GSE37142
SNP array for CNV calling AUTS2 project [Illumina]
  • Genome variation profiling by SNP array
1 Els Voorhoeve Jul 12, 2012
GSE40405
CNV and LOH analysis of patient sample PN11-0204
  • Genome variation profiling by SNP array
1 Rolph Pfundt Aug 28, 2012
GSE41297
SNP array data for embryonal rhabdomyosarcoma in a patient with Costello syndrome
1 Jan Menke Jun 12, 2015
GSE46005
Single case sample of a Non-Hodgkin lymphoma
  • Genome variation profiling by SNP array
1 Julio Finalet Apr 13, 2013
GSE47646
Generation and Characterization of an immortalized human mesenchymal stromal cell line model [Affymetrix]
1 Leonardo A. Meza-Zepeda Dec 31, 2014
GSE58694
Affymetrix CytoScan HD array data for patient with Intellectual Disabilities
1 Ruth Ruiz-Esparza Jun 21, 2014
GSE58793
De novo homozygous deletion of segmental KAL1 and entire STS cause Kallmann syndrome and X-linked ichthyosis in a Chinese family
1 Hao Xu Dec 05, 2015
GSE62438
Application of SNP-array for the detection of genomic rearrangements responsible for sindromic mental retardation of unknown cause
  • Genome variation profiling by SNP array
1 Francisco Martinez Oct 17, 2014
GSE72284
Affymetrix CytoScan 750K array data for a parthenogenetic SMA human embryonic stem cell line
  • Genome variation profiling by SNP array
1 Ephrat Levy-Lahad Sep 01, 2015
GSE100019
Loss-of-function mutations TDRD7 lead to a rare novel syndrome combining congenital cataract and non-obstructive azoospermia in humans
  • Genome variation profiling by SNP array
1 xiong bo Jun 15, 2017
GSE110235
aCGH of chromosome X in a female patient with ALL and Leri-Weill syndrome
1 Petr Vojta Feb 07, 2018