Prenatal Research CGH & CGH+SNP Microarrays - Details & Specifications
| Feature | Specification |
| Agilent Product Number | G4425B |
| Design ID | 20721 |
| Format | 2 x 105K |
| Arrays/Slide | 2 |
| Slides/Kit | 5 |
| Gene List, Annotations, Design Files, Probe Sequences | visit Agilent’s SureDesign application |
| Composition | UCSC hg19 (NCBI Build 37, February 2009) |
| Probe Spacing | |
| Manufacturing | Agilent 60-mer SurePrint technology |
| Enriched Probe Coverage | Cytogenetically relevant microdeletion, microduplication, pericentromeric and subtelomeric regions |
| Feature | Specification |
| Agilent Product Number | G5976A |
| Design ID | 36465 |
| Format | 4 x 180K |
| Arrays/Slide | 4 |
| Slides/Kit | 3 |
| Biological Features | 112841 (CGH) + 59647 (SNP) |
| Replicates of Biological Probes | 1000 |
| Internal Quality Control Features | 6,539 |
| Gene List, Annotations, Design Files, Probe Sequences | visit Agilent’s SureDesign application |
| Composition | UCSC hg19 (NCBI Build 37, February 2009) |
| Probe Spacing | 13.4 kb overall median probe spacing |
| Manufacturing | Agilent 60-mer SurePrint Technology |
| Exon-by-exon coverage of cytogenetically relevant genes | 22 |
| Enriched probe coverage | Cytogenetically relevant microdeletion, microduplication, pericentromeric and subtelomeric regions |
For Research Use Only. Not for use in diagnostic procedures