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Status
Public on Dec 01, 2015
Title
Agilent-066899 G4126A
Technology type
in situ oligonucleotide
Distribution
custom-commercial
Organism
Homo sapiens Manufacturer
Agilent Technologies
Manufacture protocol
see manufacturer's web site at http://www.agilent.com/
Description
Arrays of this design have barcodes that begin with 16066899 or 2566899
Submission date
Oct 14, 2015
Last update date
Dec 01, 2015
Contact name
Jane Houldsworth
E-mail(s)
[email protected] Phone
2015289171
Organization name
Cancer Genetics, Inc.
Street address
201 Route 17 North
City
Rutherford
State/province
NJ
ZIP/Postal code
07070
Country
USA
Samples (66)
GSM1908287 , GSM1908288 , GSM1908289 , GSM1908290 , GSM1908291 , GSM1908292
GSM1908293 ,
GSM1908294 ,
GSM1908295 ,
GSM1908296 ,
GSM1908297 ,
GSM1908298 ,
GSM1908299 ,
GSM1908300 ,
GSM1908301 ,
GSM1908302 ,
GSM1908303 ,
GSM1908304 ,
GSM1908305 ,
GSM1908306 ,
GSM1908307 ,
GSM1908308 ,
GSM1908309 ,
GSM1908310 ,
GSM1908311 ,
GSM1908312 ,
GSM1908313 ,
GSM1908314 ,
GSM1908315 ,
GSM1908316 ,
GSM1908317 ,
GSM1908318 ,
GSM1908319 ,
GSM1908320 ,
GSM1908321 ,
GSM1908322 ,
GSM1908323 ,
GSM1908324 ,
GSM1908325 ,
GSM1908326 ,
GSM1908327 ,
GSM1908328 ,
GSM1908329 ,
GSM1908330 ,
GSM1908331 ,
GSM1908332 ,
GSM1908333 ,
GSM1908334 ,
GSM1908335 ,
GSM1908336 ,
GSM1908337 ,
GSM1908338 ,
GSM1908339 ,
GSM1908340 ,
GSM1908341 ,
GSM1908342 ,
GSM1908343 ,
GSM1908344 ,
GSM1908345 ,
GSM1908346 ,
GSM1908347 ,
GSM1908348 ,
GSM1908349 ,
GSM1908350 ,
GSM1908351 ,
GSM1908352 Series (1)
GSE74025 Cross-Platform Assessment of Genomic Imbalance Confirms the Clinical Relevance of Genomic Complexity and Reveals Loci with Potential Pathogenic Roles in Diffuse Large B-Cell Lymphoma
Data table header descriptions ID Agilent feature number
CONTROL_TYPE Control type
GB_ACC GenBankAccession
GENE_SYMBOL Gene Symbol
GENE_NAME Gene Name
ACCESSION_STRING Accession String
CHROMOSOMAL_LOCATION Chromosomal Location
DESCRIPTION Description
SPOT_ID Spot identifier
Data table ID CONTROL_TYPE GB_ACC GENE_SYMBOL GENE_NAME ACCESSION_STRING CHROMOSOMAL_LOCATION DESCRIPTION SPOT_ID A_16_P21218340
FALSE
BC040319 gb|BC040319|gb|BC040319
chr21:26373084-26373143
gb|Homo sapiens hypothetical protein LOC339622, mRNA (cDNA clone IMAGE:4836841).
A_18_P13869917
FALSE
BC051441 gb|BC051441|gb|BC051441|gb|BC028044
chr21:20110035-20110094
gb|Homo sapiens cDNA clone IMAGE:6161060, partial cds.
A_16_P21031423
FALSE
HQ258093 gb|HQ258093|gb|HQ258093
chr19:51617663-51617722
A_16_P19363278
FALSE
NM_000019 entg|ACAT1
entg|acetyl-CoA acetyltransferase 1
ref|NM_000019
chr11:108005795-108005854
entg|acetyl-CoA acetyltransferase 1
A_14_P117388
FALSE
NM_000024 entg|ADRB2
entg|adrenoceptor beta 2, surface
ref|NM_000024
chr5:148207976-148208032
entg|adrenoceptor beta 2, surface
A_16_P00151888
FALSE
NM_000036 entg|AMPD1
entg|adenosine monophosphate deaminase 1
ref|NM_000036|ref|NM_001172626
chr1:115217021-115217080
entg|adenosine monophosphate deaminase 1
A_16_P19363493
FALSE
NM_000051 entg|ATM
entg|ataxia telangiectasia mutated
ref|NM_000051
chr11:108102836-108102895
entg|ataxia telangiectasia mutated
A_18_P11234465
FALSE
NM_000051 entg|ATM
entg|ataxia telangiectasia mutated
ref|NM_000051
chr11:108130266-108130325
entg|ataxia telangiectasia mutated
A_16_P39486768
FALSE
NM_000051 entg|ATM
entg|ataxia telangiectasia mutated
ref|NM_000051
chr11:108172844-108172903
entg|ataxia telangiectasia mutated
A_18_P19006806
FALSE
NM_000051 entg|ATM
entg|ataxia telangiectasia mutated
ref|NM_000051
chr11:108225441-108225500
entg|ataxia telangiectasia mutated
A_16_P19814651
FALSE
NM_000053 entg|ATP7B
entg|ATPase, Cu++ transporting, beta polypeptide
ref|NM_000053|ref|NM_001005918|ref|NM_001243182
chr13:52523783-52523842
entg|ATPase, Cu++ transporting, beta polypeptide
A_18_P19667544
FALSE
NM_000053 entg|ATP7B
entg|ATPase, Cu++ transporting, beta polypeptide
ref|NM_000053|ref|NM_001005918|ref|NM_001243182
chr13:52565251-52565310
entg|ATPase, Cu++ transporting, beta polypeptide
A_16_P16485475
FALSE
NM_000055 entg|BCHE
entg|butyrylcholinesterase
ref|NM_000055
chr3:165493838-165493897
entg|butyrylcholinesterase
A_16_P58619589
FALSE
NM_000055 entg|BCHE
entg|butyrylcholinesterase
ref|NM_000055
chr3:165542238-165542297
entg|butyrylcholinesterase
A_16_P20344959
FALSE
NM_000057 entg|BLM
entg|Bloom syndrome, RecQ helicase-like
ref|NM_000057
chr15:91267562-91267621
entg|Bloom syndrome, RecQ helicase-like
A_16_P57714698
FALSE
NM_000064 entg|C3
entg|complement component 3
ref|NM_000064
chr19:6680488-6680547
entg|complement component 3
A_16_P20949954
FALSE
NM_000064 entg|C3
entg|complement component 3
ref|NM_000064
chr19:6705206-6705265
entg|complement component 3
A_16_P18381054
FALSE
NM_000067 entg|CA2
entg|carbonic anhydrase II
ref|NM_000067
chr8:86391432-86391491
entg|carbonic anhydrase II
A_14_P112158
FALSE
NM_000067 entg|CA2
entg|carbonic anhydrase II
ref|NM_000067
chr8:86393102-86393161
entg|carbonic anhydrase II
A_16_P03425624
FALSE
NM_000068 entg|CACNA1A
entg|calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
ref|NM_000068|ref|NM_001127221|ref|NM_001127222|ref|NM_001174080|ref|NM_023035
chr19:13528819-13528878
entg|calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
23683 2652 Kbytes .Supplementary data files not provided
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