Learn about our extensive range of CGH + SNP microarrays dedicated to cytogenetic workflows. We provide whole genome CMA at variable resolutions, down to exon level, CGH+SNP arrays to analyze CN and LOH in a single experiment and application specific designs, including pre- post-natal, PGS, CNV and Cancer specific microarrays. Agilent’s CGH platform provides unmatched flexibility on content and throughput, thanks to eight different microarray formats with variable density and arrays per slide. Agilent provides a database of more than 28 million validated probes, and easy tools to customize array content based on needs. Custom or catalog, all Agilent’s CGH & CGH+SNP arrays benefit from proprietary SurePrint technology with long, high quality oligos.
GenetiSure Cyto CGH Microarrays are a set of three different microarray designs with content intended for the detection of copy number variations (CNV) only or CNV and copy-neutral loss of heterozygosity (cnLOH) in constitutional DNA samples extracted from blood, saliva, amniotic fluid or CVS.
Intended for use by cytogenetic research and clinical laboratories, this microarray is focused on disease-associated regions linked to developmental delay, intellectual disability, neuropsychiatric disorders, congenital anomalies or dysmorphic features. The 4 x 180K CGH Microarrays provides high resolution CN down exon level. The 4 x 180K CGH+SNP Microarrays provides genome wide CN and high resolution LOH down to 2.5 Mb.The 8 x 60K offers a great compromise between coverage, throughput and cost per sample.