First trimester screening (FTS) at KKH with high risk of 1:14 for trisomy 21 at week 12

Hi mummies out there.. I’ve just gotten my FTS results from KKH taken at week 12. Report shows that my baby NT 3.1 which is higher than normal 2.6. Sonographer couldn’t find baby nasal bone too. Other than that the rest of the structures are visible. During the sonogram my baby was very active and sonographer took a long time to complete my scan taking 1.5 hours. My hcg level is at 0.7 lower than normal =1. Thus this has elevated my risk for trisomy 21=1:14, trisomy 18=1:181, trisomy 13=1:889. I would like to check with mummies out there with a follow up NIPT, will the NIPT result be worse off? #1stimemom #advicepls #worriedfirsttimemom