{"product_id":"cariotipo-molecular-array-cgh-de-restos-fetales-perdida-de-embarazo","title":"Molecular karyotyping (Array CGH) of fetal remains (pregnancy loss)","description":"\u003cp\u003e This analysis can identify numerical chromosomal abnormalities, structural imbalances\u003cbr\u003e\n Genome-wide rearrangements and copy number changes, covering regions of known clinical importance (recognized microduplication\/microdeletion)\u003cbr\u003e\n syndromes), pericentromeric and subtelomeric regions, and the genomic backbone. It uses a custom-designed Illumina single nucleotide polymorphism (SNP) array. This array contains more than 630,000 SNP markers spanning both coding and non-coding sequences of the human genome. The average spatial resolution between probes is 4.5 kb.\u003c\/p\u003e","brand":"GenoLife","offers":[{"title":"Default Title","offer_id":51600447996170,"sku":"913","price":796.0,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0900\/6661\/6586\/files\/propuestas_cambio_diseno_genotica_11.png?v=1758022922","url":"https:\/\/www.genotica.com\/en\/products\/cariotipo-molecular-array-cgh-de-restos-fetales-perdida-de-embarazo","provider":"Genotica","version":"1.0","type":"link"}