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GenetiSure Postnatal Research Array (2x400K)

GenetiSure Postnatal Research Array (2x400K)


The GenetiSure postnatal research array allows simultaneous detection of copy number changes and copy neutral aberrations down to 2.5 Mb. Through the inclusion of exon-centric probes, the detection of aberrations associated with intellectual disability and congenital anomalies is maximized. The system can also be used in a wide range of postnatal array CGH research applications.

Updated CGH probe content targeted to regions of the genome known to be disease-associated can be easily sourced from the ClinGen/ISCA database.
For Research Use Only. Not for use in diagnostic procedures.

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