GenetiSure Cyto CGH & CGH+SNP Microarrays - Human Microarrays - Agilent Technology

Agilent GenetiSure Cyto CGH and CGH+SNP Microarrays offer a comprehensive solution for detecting copy number variations (CNVs) and copy-neutral loss of heterozygosity (cnLOH) in constitutional DNA samples derived from blood, saliva, amniotic fluid, or CVS. Designed for cytogenetic research and clinical laboratories, these microarrays provide reliable genomic insights for accurate interpretation of genetic abnormalities.

Focused on clinically significant, disease-associated genomic regions, the GenetiSure Cyto arrays support investigation of developmental delay, intellectual disability, neuropsychiatric disorders, congenital anomalies, and dysmorphic features.

Available Microarray Formats:

• 180K CGH Array – High-resolution copy number (CN) detection down to the exon level for precise genomic analysis.

• 180K CGH+SNP Array – Genome-wide CN detection with high-resolution LOH analysis down to 2.5 Mb, enabling comprehensive genomic profiling.

• 8x60K CGH Format – Optimized balance between genomic coverage, throughput, and cost per sample, ideal for laboratories managing multiple samples efficiently.

By combining targeted disease-region content with high-resolution performance, GenetiSure Cyto microarrays deliver dependable results for both research and clinical cytogenetic applications.

Labindia Instruments is the authorised dealer in India for Agilent Technologies, providing trusted supply and technical support for advanced genomic and cytogenetic solutions.