GSE233748[Accession] - GEO DataSets

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Items: 3

Select item 2002337481.

Affymetrix SNP array data for an INAD patient

(Submitter supplied) Infantile neuroaxonal dystrophy (INAD) is an ultra-rare early-onset autosomal recessive neurodegenerative disorder due to PLA2G6 variants. Copy number analysis of SNP arrays was performed on one INAD patient sample.

Organism:: Homo sapiens

Type:: Genome variation profiling by SNP array

Platform:: GPL18637
1 Sample

Download data: CEL, CYCHP

Series

Accession:: GSE233748

ID:: 200233748

Select item 1000186372.

[CytoScan750K_Array] Affymetrix CytoScan 750K Array

(Submitter supplied) #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 Protocol: see manufacturer's web site