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| Status |
Public on May 02, 2014 |
| Title |
[CytoScan750K_Array] Affymetrix CytoScan 750K Array |
| Technology type |
in situ oligonucleotide |
| Distribution |
commercial |
| Organism |
Homo sapiens |
| Manufacturer |
Affymetrix |
| Manufacture protocol |
see manufacturer's web site
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| |
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| Description |
#CytoScan750K_Array.cn.na32.3.annot.csv
#%create_date=2012-11-27 GMT-08:00 16:16:00
#%chip_type=CytoScan750K_Array
#%genome-species=Homo sapiens
#%genome-version=hg19
#%genome-version-ucsc=hg19
#%genome-version-ncbi=37
#%genome-version-create_date=2009-02-00
#%dbSNP_date=2010-09-23
#%dbSNP_version=132
#%dgv-date=2010-10-00
#%dgv-version=10
#%hapmap-date=2008-01-08
#%hapmap-version=23
#%netaffx-annotation-date=2012-11-05
#%netaffx-annotation-netaffx-build=32.3
#CytoScan750K_Array.na32.3.annot.csv
#%create_date=2012-11-27 GMT-08:00 16:17:00
#%chip_type=CytoScan750K_Array
#%genome-species=Homo sapiens
#%genome-version=hg19
#%genome-version-ucsc=hg19
#%genome-version-ncbi=37
#%genome-version-create_date=2009-02-00
#%dbSNP_date=2010-09-23
#%dbSNP_version=132
#%dgv-date=2010-10-00
#%dgv-version=10
#%hapmap-date=2008-01-08
#%hapmap-version=23
#%netaffx-annotation-date=2012-11-05
#%netaffx-annotation-netaffx-build=32.3
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| Web link |
http://www.affymetrix.com/support/technical/byproduct.affx?product=CytoScan750K_Array
|
| Submission date |
May 02, 2014 |
| Last update date |
Nov 21, 2014 |
| Organization |
Affymetrix, Inc. |
| E-mail(s) |
geo@ncbi.nlm.nih.gov, support@affymetrix.com
|
| Phone |
888-362-2447
|
| URL |
http://www.affymetrix.com/index.affx
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| Street address |
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| City |
Santa Clara |
| State/province |
CA |
| ZIP/Postal code |
95051 |
| Country |
USA |
| |
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| Samples (1466)
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GSM1509873, GSM1509874, GSM1509875, GSM1509876, GSM1509877, GSM1509878
GSM1509879, GSM1509880, GSM1509881, GSM1509882, GSM1509883, GSM1509884, GSM1509885, GSM1509886, GSM1509887, GSM1509888, GSM1509889, GSM1509890, GSM1509891, GSM1509892, GSM1509893, GSM1509894, GSM1509895, GSM1509896, GSM1509897, GSM1509898, GSM1509899, GSM1509900, GSM1509901, GSM1509902, GSM1509903, GSM1509904, GSM1509905, GSM1509906, GSM1509907, GSM1509908, GSM1509909, GSM1509910, GSM1509911, GSM1509912, GSM1509913, GSM1509914, GSM1509915, GSM1509916, GSM1509917, GSM1509918, GSM1509919, GSM1509920, GSM1509921, GSM1509922, GSM1509923, GSM1509924, GSM1509925, GSM1509926, GSM1509927, GSM1509928, GSM1509929, GSM1509930, GSM1509931, GSM1600223, GSM1600224, GSM1600225, GSM1600226, GSM1600227, GSM1600228, GSM1600229, GSM1600230, GSM1600231, GSM1600232, GSM1600233, GSM1600234, GSM1600235, GSM1600236, GSM1704976, GSM1726526, GSM1726527, GSM1726528, GSM1726529, GSM1726530, GSM1726531, GSM1726532, GSM1726533, GSM1726534, GSM1726535, GSM1726536, GSM1726537, GSM1726538, GSM1726539, GSM1726540, GSM1726541, GSM1859515, GSM1880582, GSM1880583, GSM1880584, GSM1880585, GSM1880586, GSM1880587, GSM1880588, GSM1880589, GSM1880590, GSM1880591, GSM1880592, GSM1880593, GSM1880594, GSM1880595, GSM1881312, GSM1881313, GSM1881314, GSM1881315, GSM1881316, GSM1881317, GSM1881318, GSM1881319, GSM1881320, GSM1881321, GSM1881322, GSM1881323, GSM1881324, GSM1881325, GSM1881326, GSM1881327, GSM1881328, GSM1881329, GSM1930162, GSM1930163, GSM1930164, GSM1930165, GSM1930166, GSM1930167, GSM1930168, GSM1930169, GSM2054048, GSM2054049, GSM2054050, GSM2054051, GSM2054052, GSM2054053, GSM2054054, GSM2054055, GSM2054056, GSM2054057, GSM2054058, GSM2054059, GSM2054060, GSM2054061, GSM2054062, GSM2054063, GSM2054064, GSM2054065, GSM2054066, GSM2054067, GSM2054068, GSM2054069, GSM2054070, GSM2054071, GSM2054072, GSM2054073, GSM2054074, GSM2054075, GSM2054076, GSM2054077, GSM2054078, GSM2054079, GSM2054080, GSM2054081, GSM2054082, GSM2054083, GSM2054084, GSM2054085, GSM2124117, GSM2124118, GSM2124119, GSM2124120, GSM2124121, GSM2667992, GSM2777095, GSM2777096, GSM2777097, GSM2777098, GSM2777099, GSM2777100, GSM3142827, GSM3142828, GSM3142829, GSM3142830, GSM3142831, GSM3142832, GSM3142833, GSM3142834, GSM3406127, GSM3406128, GSM3406129, GSM3406130, GSM3406131, GSM3406132, GSM3406133, GSM3406134, GSM3406135, GSM3406136, GSM3406137, GSM3406138, GSM3406139, GSM3406140, GSM3406141, GSM3406142, GSM3406143, GSM3406144, GSM3406145, GSM3406146, GSM3406147, GSM3406148, GSM3406149, GSM3406150, GSM3406151, GSM3406152, GSM3406153, GSM3406154, GSM3406156, GSM3406157, GSM3406158, GSM3406159, GSM3406160, GSM3406161, GSM3406162, GSM3406163, GSM3406164, GSM3406165, GSM3406166, GSM3406167, GSM3406168, GSM3406169, GSM3406170, GSM3406171, GSM3406172, GSM3406173, GSM3406174, GSM3406175, GSM3406176, GSM3406177, GSM3406178, GSM3406179, GSM3406180, GSM3406181, GSM3406182, GSM3406183, GSM3406184, GSM3406185, GSM3406186, GSM3406187, GSM3406188, GSM3406189, GSM3406190, GSM3406191, GSM3406192, GSM3406193, GSM3406194, GSM3406195, GSM3406196, GSM3406197, GSM3406198, GSM3406199, GSM3406200, GSM3406201, GSM3406202, GSM3406203, GSM3406204, GSM3406205, GSM3406206, GSM3406207, GSM3406208, GSM3406209, GSM3680599, GSM3680600, GSM3680601, GSM3680602, GSM3680603, GSM3680604, GSM3680605, GSM3680606, GSM3680607, GSM3680608, GSM3680609, GSM3680610, GSM3680611, GSM3680612, GSM3680613, GSM3680614, GSM3680615, GSM3680616, GSM3680617, GSM3680618, GSM3680619, GSM3680620, GSM3680621, GSM3680622, GSM3680623, GSM3680624, GSM4107987, GSM4107988, GSM4107989, GSM4610644, GSM4610645, GSM4610646, GSM4610647, GSM4610648, GSM4610649, GSM4610650, GSM4610651, GSM4610652, GSM4610653, GSM4819870, GSM4819871, GSM4819872, GSM4987616, GSM4987617, GSM4987618, GSM4987619, GSM4987620, GSM4987621, GSM4987622, GSM4987623, GSM4987624, GSM4987625, GSM4987626, GSM4987627, GSM4987628, GSM4987629, GSM4987630, GSM4987631, GSM4987632, GSM4987633, GSM4987634, GSM4987635, GSM4987636, GSM4987637, GSM4987638, GSM5206729, GSM5206730, GSM5356863, GSM5356864, GSM5508159, GSM5597156, GSM5597157, GSM6157174, GSM6157175, GSM6157176, GSM6157177, GSM6157178, GSM6157179, GSM6157180, GSM6157181, GSM6157182, GSM6157183, GSM6157184, GSM6157185, GSM6157186, GSM6157187, GSM6157188, GSM6157189, GSM6157190, GSM6157191, GSM6157192, GSM6157193, GSM6157194, GSM6157195, GSM6157196, GSM6157197, GSM6157198, GSM6157199, GSM6157200, GSM6157201, GSM6157202, GSM6157203, GSM6157204, GSM6157205, GSM6321992, GSM6321993, GSM6321994, GSM6321995, GSM6321996, GSM6321997, GSM6321998, GSM6321999, GSM6322000, GSM6322001, GSM6322002, GSM6322003, GSM6322004, GSM6322005, GSM6322006, GSM6322007, GSM6322008, GSM6322009, GSM6322010, GSM6322011, GSM6322012, GSM6322013, GSM6322014, GSM6322015, GSM6322016, GSM6322017, GSM6322018, GSM6322019, GSM6322020, GSM6322021, GSM6322022, GSM6322023, GSM6322024, GSM6322025, GSM6322026, GSM6322027, GSM6322028, GSM6322029, GSM6322030, GSM6322031, GSM6322032, GSM6322033, GSM6322034, GSM6322035, GSM6322036, GSM6322037, GSM6322038, GSM6322039, GSM6322040, GSM6322041, GSM6322042, GSM6322043, GSM6322044, GSM6322045, GSM6322046, GSM6322047, GSM6322048, GSM6322049, GSM6322050, GSM6322051, GSM6322052, GSM6322053, GSM6322054, GSM6322055, GSM6322056, GSM6322057, GSM6322058, GSM6322059, GSM6322060, GSM6322061, GSM6322062, GSM6322063, GSM6322064, GSM6322065, GSM6322066, GSM6322067, GSM6322068, GSM6322069, GSM6322070, GSM6322071, GSM6322072, GSM6322073, GSM6322074, GSM6322075, GSM6322076, GSM6322077, GSM6322078, GSM6322079, GSM6322080, GSM6322081, GSM6322082, GSM6322083, GSM6322084, GSM6322085, GSM6322086, GSM6322087, GSM6322088, GSM6322089, GSM6322090, GSM6322091, GSM6322092, GSM6322093, GSM6322094, GSM6322095, GSM6322096, GSM6322097, GSM6322098, GSM6322099, GSM6322100, GSM6322101, GSM6322102, GSM6322103, GSM6322104, GSM6322105, GSM6322106, GSM6322107, GSM6322108, GSM6322109, GSM6322110, GSM6322111, GSM6322112, GSM6322113, GSM6322114, GSM6322115, GSM6322116...
Accession list truncated, click here to browse through all related public accessions
You can also download a list of all accessions here
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| Series (42)
|
| GSE61650 |
The cellular origin and malignant transformation of Waldenström's Macroglobulinemia [copy number variation] |
| GSE61651 |
The cellular origin and malignant transformation of Waldenström's Macroglobulinemia |
| GSE65569 |
Altered integrin expression patterns revealed by microarray in matched human melanomas (snp) |
| GSE65570 |
CNV and expression patterns in matched human melanoma tissues and cell lines with different invasive property. |
| GSE69632 |
Effects of Integrating and Non-integrating Reprogramming Methods on Copy Number Variation and Genomic Stability of Human Induced Pluripotent Stem Cells |
| GSE70397 |
Phenotypic and genomic analysis of multiple myeloma minimal residual disease clonal plasma cells: a new model to understand chemoresistance [CytoScan750K Copy Number, LOH] |
| GSE70399 |
Phenotypic and genomic analysis of multiple myeloma minimal residual disease clonal plasma cells: a new model to understand chemoresistance |
| GSE72284 |
Affymetrix CytoScan 750K array data for a parthenogenetic SMA human embryonic stem cell line |
| GSE73005 |
Affymetrix SNP array data for myelodysplastic syndromes (MDS) samples |
| GSE73041 |
Phenotypic, transcriptomic and genomic characterization of clonal plasma cells in light chain amyloidosis [Copy number analysis] |
| GSE73042 |
Phenotypic, transcriptomic and genomic characterization of clonal plasma cells in light chain amyloidosis |
| GSE77536 |
Integrative analysis of DNA copy number, DNA methylation and gene expression in multiple myeloma reveals alterations related to relapse [DNA copy number] |
| GSE77540 |
Integrative analysis of DNA copy number, DNA methylation and gene expression in multiple myeloma reveals alterations related to relapse |
| GSE80314 |
Immunophenotypic and detailed cytogenetic characterization of cell lines derived from myelodysplastic syndrome patients after progression to acute myeloid leukemia |
| GSE100019 |
Loss-of-function mutations TDRD7 lead to a rare novel syndrome combining congenital cataract and non-obstructive azoospermia in humans |
| GSE103636 |
Human embryonic stem cells in AKIT, E8 and KSR/bFGF culture medium |
| GSE103669 |
Growth factor-free, chemically-defined culture system for expansion and derivation of human pluripotent stem cells |
| GSE114488 |
CNV patterns in BRAFi resistant melanoma cell lines |
| GSE120624 |
Affymetrix CytoScan 750K and HD data for developmental delay and/or physical disability phenotypes samples |
| GSE128583 |
Chromothripsis is a prognostic factor in early-onset breast cancer [CytoScan750K_Array] |
| GSE128587 |
Chromothripsis is a prognostic factor in early-onset breast cancer |
| GSE138438 |
Copy-number profiling by SNP array of 4 acute myeloid leukemia (AML) cell lines |
| GSE152288 |
Affymetrix CytoScan 750K data for validation of the BoBs/CNV-seq comparison study |
| GSE159129 |
Clinical and molecular characterization of patients with 16p11.2 microdeletion syndrome |
| GSE163799 |
Evaluation of chromosomal abnormalities and copy number variations in fetuses with ultrasonic soft markers |
| GSE169469 |
11p11.12p12 duplication in a family with intellectual disability and craniofacial anomalies |
| GSE176138 |
A prenatal diagnosis case of partial duplication 21q21.1-q21.2 with normal phenotype maternally inherited |
| GSE181612 |
CytoScan 750K array data for the ataxia patient's sample |
| GSE184764 |
Divergent leukemia subclones as cellular models for testing vulnerabilities associated with gains in chromosomes 7, 8 or 18 |
| GSE203126 |
Chromosomal abnormalities and pregnancy outcomes for fetuses with gastrointestinal tract obstructions |
| GSE207887 |
Chromosomal abnormalities of 564 miscarriages |
| GSE208291 |
Prenatal diagnosis of genetic aberrations in fetuses with pulmonary stenosis using ultrasound in Southern China |
| GSE208389 |
Retrospective study of 186 fetuses with sex chromosomal copy number variations |
| GSE211577 |
Fetal genetic findings for fetal growth restriction without structural malformations at a territory referral center: 10-year experience |
| GSE212870 |
Array46 750k test is an in-depht analysis to detect chromosomal alterations, CNVs and SNPs |
| GSE213813 |
Affymetrix SNP array data for induced pluripotent stem cell line |
| GSE223242 |
Genetic analysis, ultrasound phenotype, and pregnancy outcome of fetuses with Xp22.33 or Yp11.32 microdeletion |
| GSE230532 |
Prenatal Diagnosis and Clinical Analysis of Talipes Equinovarus by Chromosomal Microarray Analysis |
| GSE230763 |
Can non-invasive prenatal screening based on cell-free fetal DNA be utilized to assess chromosome abnormalities in fetuses with increased Nuchal Translucency? |
| GSE233748 |
Affymetrix SNP array data for an INAD patient |
| GSE235430 |
Ultrasonographic characteristics, genetic features, and maternal and fetal outcomes in fetuses with omphalocele: a single tertiary center experience |
| GSE240611 |
Prenatal phenotypes and pregnancy outcomes of fetuses with recurrent 1q21.1 microdeletions and microduplications |
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| Supplementary file |
Size |
Download |
File type/resource |
| GPL18637_CytoScan750K_Array.cn.na32.3.annot.csv.gz |
34.0 Mb |
(ftp)(http) |
CSV |
| GPL18637_CytoScan750K_Array.na32.3.annot.csv.gz |
67.5 Mb |
(ftp)(http) |
CSV |
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