|
| Status |
Public on Jul 12, 2012 |
| Title |
Oligo array for CNV calling AUTS2 project [Agilent] |
| Organism |
Homo sapiens |
| Experiment type |
Genome variation profiling by genome tiling array
|
| Summary |
Phenotypic and genotypic description of AUTS2 deletion patients found by Array analysis in an international cohort of intellectual disability (ID) and multiple congenital malformations (MCA).
|
| |
|
| Overall design |
Arrays were hybridized and analysed using manufacturer's protocols on DNA from patients with ID/MCA
|
| |
|
| Contributor(s) |
van Binsbergen E, Voorhoeve E, Beunders G |
| Citation(s) |
23332918 |
| Submission date |
Apr 10, 2012 |
| Last update date |
Jan 29, 2015 |
| Contact name |
Els Voorhoeve |
| E-mail(s) |
e.voorhoeve@vumc.nl
|
| Phone |
+31204440157
|
| Organization name |
VU medical center
|
| Department |
Clinical Genetics
|
| Lab |
Cytogenetics
|
| Street address |
De Boelelaan 1117
|
| City |
Amsterdam |
| ZIP/Postal code |
1081 HV |
| Country |
Netherlands |
| |
|
| Platforms (1) |
| GPL8693 |
Agilent-019015 HD CGH Microarray (2X105K) Oxford design AMADID#019015 (Feature number version) |
|
| Samples (2) |
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| This SubSeries is part of SuperSeries: |
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| Relations |
| BioProject |
PRJNA170382 |
